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- [21] Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypesClinical and Experimental Nephrology, 2022, 26 : 140 - 153Shinya Ishiko论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsNaoya Morisada论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsAtsushi Kondo论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsSadayuki Nagai论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsYuya Aoto论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsEri Okada论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsRini Rossanti论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsNana Sakakibara论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsChina Nagano论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsTomoko Horinouchi论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsTomohiko Yamamura论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsTakeshi Ninchoji论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsHiroshi Kaito论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsRiku Hamada论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsYuko Shima论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsKoichi Nakanishi论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsMasafumi Matsuo论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsKazumoto Iijima论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of PediatricsKandai Nozu论文数: 0 引用数: 0 h-index: 0机构: Kobe University Graduate School of Medicine,Department of Pediatrics
- [22] Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variantsKIDNEY INTERNATIONAL, 2021, 100 (03) : 650 - 659Burgmaier, Kathrin论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Dept Pediat, Cologne, Germany Univ Hosp Cologne, Ctr Rare Dis, Cologne, Germany Univ Cologne, Fac Med, Cologne, GermanyBrinker, Leonie论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Dept Pediat, Cologne, Germany Univ Cologne, Fac Med, Cologne, GermanyErger, Florian论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Ctr Rare Dis, Cologne, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, Germany Univ Cologne, Fac Med, Univ Hosp Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Fac Med, Cologne, GermanyBeck, Bodo B.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Ctr Rare Dis, Cologne, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, Germany Univ Cologne, Fac Med, Univ Hosp Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Fac Med, Cologne, GermanyBenz, Marcus R.论文数: 0 引用数: 0 h-index: 0机构: Pediat Nephrol Dachau, Dachau, Germany Univ Cologne, Fac Med, Cologne, GermanyBergmann, Carsten论文数: 0 引用数: 0 h-index: 0机构: Med Genet Mainz, Limbach Genet, Mainz, Germany Univ Freiburg, Div Renal, Dept Med, Med Ctr, Freiburg, Germany Univ Cologne, Fac Med, Cologne, GermanyBoyer, Olivia论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Necker Hosp, APHP, Dept Pediat Nephrol & Kidney Transplantat, Paris, France Univ Cologne, Fac Med, Cologne, GermanyCollard, Laure论文数: 0 引用数: 0 h-index: 0机构: Clin Esperance, Reference Ctr Pediat Nephrol, Montegnee, Belgium IRCCS, Bambino Gesu Childrens Hosp, Dept Pediat Subspecialties, Div Nephrol, Rome, Italy Univ Cologne, Fac Med, Cologne, GermanyDafinger, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Cologne, Fac Med, Univ Hosp Cologne, Ctr Mol Med Cologne, Cologne, Germany Childrens Mem Hlth Inst, Dept Nephrol Kidney Transplantat & Hypert, Warsaw, Poland Univ Cologne, Fac Med, Cologne, Germany论文数: 引用数: h-index:机构:Kowalewska, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, GermanyLange-Sperandio, Baerbel论文数: 0 引用数: 0 h-index: 0机构: LMU, Univ Hosp, Dr Hauner Childrens Hosp, Dept Pediat, Munich, Germany Univ Cologne, Fac Med, Cologne, GermanyMassella, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, GermanyMastrangelo, Antonio论文数: 0 引用数: 0 h-index: 0机构: Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Pediatr Nephrol Dialysis & Transplant Unit, Milan, Italy Univ Cologne, Fac Med, Cologne, GermanyMekahli, Djalila论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Dev & Regenerat, PKD Res Grp, Leuven, Belgium Univ Hosp Leuven, Dept Pediat Nephrol, Leuven, Belgium Univ Cologne, Fac Med, Cologne, GermanyMiklaszewska, Monika论文数: 0 引用数: 0 h-index: 0机构: Jagiellonian Univ Med Coll, Dept Pediat Nephrol & Hypertens, Fac Med, Krakow, Poland Univ Cologne, Fac Med, Cologne, GermanyOrtiz-Bruechle, Nadina论文数: 0 引用数: 0 h-index: 0机构: RWTH Univ, Hosp Aachen, Inst Human Genet, Aachen, Germany Univ Cologne, Fac Med, Cologne, GermanyPatzer, Ludwig论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp St Elisabeth & St Barbara, Dept Pediat, Halle, Germany Univ Cologne, Fac Med, Cologne, GermanyPrikhodina, Larisa论文数: 0 引用数: 0 h-index: 0机构: Pirogov Russian Natl Res Med Univ, Res Clin Inst Pediat Acad Y E Veltishev, Dept Inherited & Acquired Kidney Dis, Moscow, Russia Univ Cologne, Fac Med, Cologne, GermanyRanchin, Bruno论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Hop Femme Mere Enfant, Pediat Nephrol Unit, Ctr Reference Malad Renales Rares, Bron, France Univ Cologne, Fac Med, Cologne, GermanyRanguelov, Nadejda论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Dept Pediat, Sch Med, St Luc Acad Hosp, Brussels, Belgium Univ Cologne, Fac Med, Cologne, GermanySchild, Raphael论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Hamburg Eppendorf, Univ Childrens Hosp, Hamburg, Germany Univ Cologne, Fac Med, Cologne, Germany论文数: 引用数: h-index:机构:Sever, Lale论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ Cerrahpasa, Cerrahpasa Sch Med, Dept Pediat Nephrol, Istanbul, Turkey Univ Cologne, Fac Med, Cologne, GermanySikora, Przemyslaw论文数: 0 引用数: 0 h-index: 0机构: Med Univ Lublin, Dept Pediat Nephrol, Lublin, Poland Univ Cologne, Fac Med, Cologne, GermanySzczepanska, Maria论文数: 0 引用数: 0 h-index: 0机构: Med Univ Silesia, Fac Med Sci Zabrze, Dept Pediat, Katowice, Poland Univ Cologne, Fac Med, Cologne, GermanyTeixeira, Ana论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Porto, Ctr Materno Infantil Norte, Porto, Portugal Univ Cologne, Fac Med, Cologne, GermanyThumfart, Julia论文数: 0 引用数: 0 h-index: 0机构: Charite, Dept Pediat Gastroenterol Nephrol & Metab D, Berlin, Germany Univ Cologne, Fac Med, Cologne, GermanyUetz, Barbara论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Munich Schwabing, KfH Ctr Pediat Nephrol, Munich, Germany Univ Cologne, Fac Med, Cologne, GermanyWeber, Lutz Thorsten论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Dept Pediat, Cologne, Germany Univ Hosp Cologne, Ctr Rare Dis, Cologne, Germany Univ Cologne, Fac Med, Cologne, GermanyWuehl, Elke论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, GermanyZerres, Klaus论文数: 0 引用数: 0 h-index: 0机构: RWTH Univ, Hosp Aachen, Inst Human Genet, Aachen, Germany Univ Cologne, Fac Med, Cologne, GermanyDoetsch, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Dept Pediat, Cologne, Germany Univ Hosp Cologne, Ctr Rare Dis, Cologne, Germany Univ Cologne, Fac Med, Cologne, Germany论文数: 引用数: h-index:机构:Liebau, Max Christoph论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne, Germany Univ Hosp Cologne, Dept Pediat, Cologne, Germany Univ Hosp Cologne, Ctr Rare Dis, Cologne, Germany Univ Cologne, Fac Med, Univ Hosp Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Fac Med, Cologne, Germany
- [23] Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypesCLINICAL AND EXPERIMENTAL NEPHROLOGY, 2022, 26 (02) : 140 - 153Ishiko, Shinya论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanMorisada, Naoya论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Hyogo Prefectural Kobe Childrens Hosp, Dept Clin Genet, Chou Ku, 1-6-7 Minatojimaminami Machi, Kobe, Hyogo 6500047, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanKondo, Atsushi论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanNagai, Sadayuki论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanAoto, Yuya论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan论文数: 引用数: h-index:机构:Rossanti, Rini论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan论文数: 引用数: h-index:机构:Nagano, China论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanHorinouchi, Tomoko论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanYamamura, Tomohiko论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan论文数: 引用数: h-index:机构:Kaito, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Hyogo Prefectural Kobe Childrens Hosp, Dept Nephrol, Chou Ku, 1-6-7 Minatojimaminami Machi, Kobe, Hyogo 6500047, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanHamada, Riku论文数: 0 引用数: 0 h-index: 0机构: Tokyo Metropolitan Childrens Med Ctr, Dept Nephrol, 2-8-29 Musashidai, Fichu, Tokyo 1838561, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, JapanShima, Yuko论文数: 0 引用数: 0 h-index: 0机构: Wakayama Med Univ, Dept Pediat, 811-1 Kimiidera, Wakayama, Wakayama 6418509, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Iijima, Kazumoto论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan Kobe Univ, Dept Pediat, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan论文数: 引用数: h-index:机构:
- [24] A clinical test by direct fluorescent DNA sequencing of the PKHD1 gene in autosomal-recessive polycystic kidney disease (ARPKD)JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (05): : 629 - 629Courteau, L. K.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin Rochester, Mol Genet, Rochester, MN USA Mayo Clin Rochester, Mol Genet, Rochester, MN USAConsugar, M.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin Rochester, Mol Genet, Rochester, MN USA Mayo Clin Rochester, Mol Genet, Rochester, MN USAButz, M.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin Rochester, Mol Genet, Rochester, MN USA Mayo Clin Rochester, Mol Genet, Rochester, MN USARossetti, S.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin Rochester, Mol Genet, Rochester, MN USA Mayo Clin Rochester, Mol Genet, Rochester, MN USAHarris, P.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin Rochester, Mol Genet, Rochester, MN USA Mayo Clin Rochester, Mol Genet, Rochester, MN USAThibodeau, S.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin Rochester, Mol Genet, Rochester, MN USA Mayo Clin Rochester, Mol Genet, Rochester, MN USA
- [25] Exome sequencing identifies compound heterozygous PKHD1 mutations as a cause of autosomal recessive polycystic kidney diseaseCHINESE MEDICAL JOURNAL, 2012, 125 (14) : 2482 - 2486Zhang Da论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaLu Lin论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Peking Union Med Coll, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaYang Hong-bo论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaLi Mei论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaSun Hao论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Radiol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaZeng Zheng-pei论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaLi Xin-ping论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaXia Wei-bo论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaXing Xiao-ping论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Peking Union Med Coll Hosp, Beijing 100730, Peoples R China
- [26] Clinical and pathological features of a neonate with autosomal recessive polycystic kidney disease caused by a nonsense PKHD1 mutationWORLD JOURNAL OF PEDIATRICS, 2013, 9 (01) : 76 - 79Zhou, Xi-Hui论文数: 0 引用数: 0 h-index: 0机构: Xi An Jiao Tong Univ, Key Lab Environm & Genes Related Dis, Affiliated Hosp 1, Dept Neonatol,Sch Med,Ion Channel Dis Lab,Minist, Xian 710061, Peoples R China Xi An Jiao Tong Univ, Key Lab Environm & Genes Related Dis, Affiliated Hosp 1, Dept Neonatol,Sch Med,Ion Channel Dis Lab,Minist, Xian 710061, Peoples R ChinaHui, Zhi-Yan论文数: 0 引用数: 0 h-index: 0机构: Xi An Jiao Tong Univ, Key Lab Environm & Genes Related Dis, Affiliated Hosp 1, Dept Neonatol,Sch Med,Ion Channel Dis Lab,Minist, Xian 710061, Peoples R China Xi An Jiao Tong Univ, Key Lab Environm & Genes Related Dis, Affiliated Hosp 1, Dept Neonatol,Sch Med,Ion Channel Dis Lab,Minist, Xian 710061, Peoples R ChinaLi, Yuan论文数: 0 引用数: 0 h-index: 0机构: Xi An Jiao Tong Univ, Key Lab Environm & Genes Related Dis, Affiliated Hosp 1, Dept Neonatol,Sch Med,Ion Channel Dis Lab,Minist, Xian 710061, Peoples R China Xi An Jiao Tong Univ, Key Lab Environm & Genes Related Dis, Affiliated Hosp 1, Dept Neonatol,Sch Med,Ion Channel Dis Lab,Minist, Xian 710061, Peoples R China
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