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- [41] Whole exome sequencing reveals novel COL4A3 and COL4A4mutations and resolves diagnosis in Chinese families with kidney diseaseBMC Nephrology, 15Fujun Lin论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalFan Bian论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalJun Zou论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalXiangru Wu论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalJianping Shan论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalWei Lu论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalYao Yao论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalGengru Jiang论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua HospitalDaniel Philip Gale论文数: 0 引用数: 0 h-index: 0机构: School of Medicine,Department of Nephrology, Xin Hua Hospital
- [42] Identification of novel SHANK2 variants in two Chinese families via exome and RNA sequencingFRONTIERS IN NEUROSCIENCE, 2023, 17Wu, Yong论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R China Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R ChinaLi, Wenzhou论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R China Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R ChinaTan, Bo论文数: 0 引用数: 0 h-index: 0机构: Chongqing Med Univ, Affiliated Hosp 2, Dept Obstet & Gynecol, Chongqing, Peoples R China Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R ChinaLuo, Sanchuan论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R China Shenzhen Baoan Womens & Childrens Hosp, Med Res Inst, Shenzhen, Peoples R China
- [43] Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney diseaseBMC NEPHROLOGY, 2014, 15Lin, Fujun论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Royal Free Hosp, UCL Ctr Nephrol, London NW3 2QG, England Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaBian, Fan论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaZou, Jun论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaWu, Xiangru论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Pathol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaShan, Jianping论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaLu, Wei论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaYao, Yao论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaJiang, Gengru论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R ChinaGale, Daniel Philip论文数: 0 引用数: 0 h-index: 0机构: Royal Free Hosp, UCL Ctr Nephrol, London NW3 2QG, England Shanghai Jiao Tong Univ, Xin Hua Hosp, Sch Med, Dept Nephrol, Shanghai 200030, Peoples R China
- [44] Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (vol 101, pg 789, 2017)AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (06) : 1034 - 1034Sanna-Cherchi, Simone论文数: 0 引用数: 0 h-index: 0Khan, Kamal论文数: 0 引用数: 0 h-index: 0Westland, Rik论文数: 0 引用数: 0 h-index: 0Krithivasan, Priya论文数: 0 引用数: 0 h-index: 0Fievet, Lorraine论文数: 0 引用数: 0 h-index: 0Rasouly, Hila Milo论文数: 0 引用数: 0 h-index: 0Ionita-Laza, Iuliana论文数: 0 引用数: 0 h-index: 0Capone, Valentina P.论文数: 0 引用数: 0 h-index: 0Fasel, David A.论文数: 0 引用数: 0 h-index: 0Kiryluk, Krzysztof论文数: 0 引用数: 0 h-index: 0Kamalakaran, Sitharthan论文数: 0 引用数: 0 h-index: 0Bodria, Monica论文数: 0 引用数: 0 h-index: 0Otto, Edgar A.论文数: 0 引用数: 0 h-index: 0Sampson, Matthew G.论文数: 0 引用数: 0 h-index: 0Gillies, Christopher E.论文数: 0 引用数: 0 h-index: 0Vega-Warner, Virginia论文数: 0 引用数: 0 h-index: 0Vukojevic, Katarina论文数: 0 引用数: 0 h-index: 0Pediaditakis, Igor论文数: 0 引用数: 0 h-index: 0Makar, Gabriel S.论文数: 0 引用数: 0 h-index: 0Mitrotti, Adele论文数: 0 引用数: 0 h-index: 0Verbitsky, Miguel论文数: 0 引用数: 0 h-index: 0Martino, Jeremiah论文数: 0 引用数: 0 h-index: 0Liu, Qingxue论文数: 0 引用数: 0 h-index: 0Na, Young-Ji论文数: 0 引用数: 0 h-index: 0Goj, Vinicio论文数: 0 引用数: 0 h-index: 0Ardissino, Gianluigi论文数: 0 引用数: 0 h-index: 0Gigante, Maddalena论文数: 0 引用数: 0 h-index: 0Gesualdo, Loreto论文数: 0 引用数: 0 h-index: 0Janezcko, Magdalena论文数: 0 引用数: 0 h-index: 0Zaniew, Marcin论文数: 0 引用数: 0 h-index: 0Mendelsohn, Cathy Lee论文数: 0 引用数: 0 h-index: 0Shril, Shirlee论文数: 0 引用数: 0 h-index: 0Hildebrandt, Friedhelm论文数: 0 引用数: 0 h-index: 0van Wijk, Joanna A. E.论文数: 0 引用数: 0 h-index: 0Arapovic, Adela论文数: 0 引用数: 0 h-index: 0Saraga, Marijan论文数: 0 引用数: 0 h-index: 0Allegri, Landino论文数: 0 引用数: 0 h-index: 0Izzi, Claudia论文数: 0 引用数: 0 h-index: 0Scolari, Francesco论文数: 0 引用数: 0 h-index: 0Tasic, Velibor论文数: 0 引用数: 0 h-index: 0Ghiggeri, Gian Marco论文数: 0 引用数: 0 h-index: 0Latos-Bielenska, Anna论文数: 0 引用数: 0 h-index: 0Materna-Kiryluk, Anna论文数: 0 引用数: 0 h-index: 0Mane, Shrikant论文数: 0 引用数: 0 h-index: 0Goldstein, David B.论文数: 0 引用数: 0 h-index: 0Lifton, Richard P.论文数: 0 引用数: 0 h-index: 0Katsanis, Nicholas论文数: 0 引用数: 0 h-index: 0Davis, Erica E.论文数: 0 引用数: 0 h-index: 0Gharavi, Ali G.论文数: 0 引用数: 0 h-index: 0
- [45] X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypesOrphanet Journal of Rare Diseases, 9Anju K Philips论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteAuli Sirén论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteKristiina Avela论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteMirja Somer论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteMaarit Peippo论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteMinna Ahvenainen论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteFatma Doagu论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteMaria Arvio论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteHelena Kääriäinen论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteHilde Van Esch论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteGuy Froyen论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteStefan A Haas论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteHao Hu论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteVera M Kalscheuer论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman InstituteIrma Järvelä论文数: 0 引用数: 0 h-index: 0机构: University of Helsinki,Department of Medical Genetics, Haartman Institute
- [46] X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypesORPHANET JOURNAL OF RARE DISEASES, 2014, 9Philips, Anju K.论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandSiren, Auli论文数: 0 引用数: 0 h-index: 0机构: Tampere Univ Hosp, Outpatient Clin Persons Intellectual Disabil, Tampere, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandAvela, Kristiina论文数: 0 引用数: 0 h-index: 0机构: Norio Ctr, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandSomer, Mirja论文数: 0 引用数: 0 h-index: 0机构: Norio Ctr, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandPeippo, Maarit论文数: 0 引用数: 0 h-index: 0机构: Norio Ctr, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandAhvenainen, Minna论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandDoagu, Fatma论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandArvio, Maria论文数: 0 引用数: 0 h-index: 0机构: Paijat Hame Cent Hosp, Lahti, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandKaariainen, Helena论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Cent Hosp, Dept Clin Genet, Helsinki, Finland Natl Inst Hlth & Welf, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandVan Esch, Hilde论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Ctr Human Genet, Louvain, Belgium Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandFroyen, Guy论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, VIB Ctr Biol Dis, Dept Human Genet, Human Genome Lab, Louvain, Belgium Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandHaas, Stefan A.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Mol Genet, Dept Computat Mol Biol, D-14195 Berlin, Germany Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandHu, Hao论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Mol Genet, Dept Human Mol Genet, D-14195 Berlin, Germany Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandKalscheuer, Vera M.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Mol Genet, Dept Human Mol Genet, D-14195 Berlin, Germany Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, FinlandJarvela, Irma论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, Finland Univ Helsinki, Haartman Inst, Dept Med Genet, Helsinki, Finland
- [47] Novel Mutations in Chinese Patients with Multiple Osteochondromas Identified Using Whole Exome SequencingGENETIC TESTING AND MOLECULAR BIOMARKERS, 2021, 25 (05) : 361 - 367Tong, Yu论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Zhejiang, Peoples R China Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Dept Orthoped Surg, Peoples Hosp, Hangzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaLuo, Junchao论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaZhang, Yin论文数: 0 引用数: 0 h-index: 0机构: Bengbu Med Coll, Grad Dept, Bengbu, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaHong, Zheping论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Dept Orthoped Surg, Peoples Hosp, Hangzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaCao, Li论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Dept Orthoped Surg, Peoples Hosp, Hangzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaChen, Xinji论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Dept Orthoped Surg, Peoples Hosp, Hangzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaChen, Jihang论文数: 0 引用数: 0 h-index: 0机构: Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Dept Orthoped Surg, Peoples Hosp, Hangzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R ChinaBi, Qing论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Zhejiang, Peoples R China Hangzhou Med Coll, Zhejiang Prov Peoples Hosp, Dept Orthoped Surg, Peoples Hosp, Hangzhou, Zhejiang, Peoples R China Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Zhejiang, Peoples R China
- [48] Whole-exome sequencing identified two novel mutations of DYNC2LI1 in fetal skeletal ciliopathyMOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (12):Zhang, Xinyue论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaYou, Yanqin论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaXie, Xiaoxiao论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaXu, Hong论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Ultrasound, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaZhou, Honghui论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaLei, Yuanmei论文数: 0 引用数: 0 h-index: 0机构: Peoples Liberat Army Gen Hosp, Med Ctr Chinese 1, Dept Dermatol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaSun, Pei论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaMeng, Yuanguang论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaWang, Longxia论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Ultrasound, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R ChinaLu, Yanping论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Obstet & Gynecol, Beijing, Peoples R China
- [49] Case Report: Whole Exome Sequencing Revealed Two Novel Mutations of PIEZO1 Implicated in Nonimmune Hydrops FetalisFRONTIERS IN GENETICS, 2021, 12Chen, Yuan论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaJiang, Ying论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaChen, Bangwu论文数: 0 引用数: 0 h-index: 0机构: Ninghai Maternal & Child Hlth Care Hosp, Dept Obstet, Ningbo, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaQian, Yeqing论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Dept Reprod Genet, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaLiu, Jiao论文数: 0 引用数: 0 h-index: 0机构: Lishui Maternal & Child Hlth Care Hosp, Dept Obstet, Lishui, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaYang, Mengmeng论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaZhao, Baihui论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaLuo, Qiong论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China
- [50] Correction to: Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic NeuropathiesJournal of Molecular Neuroscience, 2020, 70 : 631 - 631Xiao-Huan Zou论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyXin-Xin Guo论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyHui-Zhen Su论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyChong Wang论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyEn-Lin Dong论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyNing Wang论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyWan-Jin Chen论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of NeurologyQi-Jie Zhang论文数: 0 引用数: 0 h-index: 0机构: First Affiliated Hospital of Fujian Medical University,Department of Neurology and Institute of Neurology