Biallelic mutations in UGDH cause congenital microcephaly

被引:1
|
作者
Shu, Li [1 ,2 ,3 ,4 ,5 ]
Xie, Guangyao [1 ]
Mei, Daoqi [6 ]
Xu, Rui [7 ]
Liu, Shixian [8 ]
Xiao, Bo [9 ]
Li, Xing [10 ]
Xie, Yuanyuan [9 ]
Mao, Xiao [1 ,11 ,12 ]
Wang, Hua [13 ]
机构
[1] Hunan Prov Maternal & Child Hlth Care Hosp, Natl Hlth Commiss Key Lab Birth Defect Res & Prev, Changsha 410005, Hunan, Peoples R China
[2] Univ Calgary, Cumming Sch Med, Dept Biochem, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Cumming Sch Med, Dept Mol Biol, Calgary, AB T2N 4N1, Canada
[4] Univ Calgary, Cumming Sch Med, Dept Med Genet, Calgary, AB T2N 4N1, Canada
[5] Univ Calgary, Alberta Childrens Hosp, Res Inst, Calgary, AB T2N 4N1, Canada
[6] Zhengzhou Univ, Dept Neurol, Childrens Hosp, Zhengzhou 450018, Henan, Peoples R China
[7] Xinjiang Med Univ, Sch Basic Med Sci, Dept Cell Biol & Genet, Urumqi 830054, Xinjiang, Peoples R China
[8] Ganzhou Women & Childrens Hlth Care Hosp, Dept Pediat Neurol & Rehabil, Ganzhou 341000, Jiangxi, Peoples R China
[9] Xiangya Hosp, Dept Neurol, Changsha 410005, Hunan, Peoples R China
[10] Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning 530021, Guangxi, Peoples R China
[11] Hunan Prov Maternal & Child Hlth Care Hosp, Dept Med Genet, Changsha 410005, Hunan, Peoples R China
[12] Hunan Prov Maternal & Child Hlth Care Hosp, Clin Res Ctr Placental Med Hunan Prov, Changsha 410005, Hunan, Peoples R China
[13] Hunan Childrens Hosp, Dept Med Genet, Changsha 410007, Hunan, Peoples R China
关键词
GENE;
D O I
10.1016/j.gendis.2022.12.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:1816 / 1819
页数:4
相关论文
共 50 条
  • [21] UGDH germline loss-of-function mutations cause epilepsy and global developmental delay
    Bosso-Lefevre, Celia
    Yu, Emily
    Grady, George
    Szenker, Emmanuelle
    Jamuar, Saumya S.
    Muriello, Michael
    Gunay-Aygun, Meral
    Koolen, David
    Lefeber, Dirk
    Hengel, Holger
    Schoels, Ludger
    Simpson, Melanie
    Ciruna, Brian
    Reversade, Bruno
    MECHANISMS OF DEVELOPMENT, 2017, 145 : S26 - S27
  • [22] Biallelic mutations in PMFBP1 cause acephalic spermatozoa
    Sha, Yan-Wei
    Wang, Xiong
    Xu, Xiaohui
    Ding, Lu
    Liu, Wen-Sheng
    Li, Ping
    Su, Zhi-Ying
    Chen, Jing
    Mei, Li-Bin
    Zheng, Liang-Kai
    Wang, Hai-Long
    Kong, Shuang-Bo
    You, Min
    Wu, Jian-Feng
    CLINICAL GENETICS, 2019, 95 (02) : 277 - 286
  • [23] Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C
    Reinstein, Eyal
    Gutierrez-Fernandez, Ana
    Tzur, Shay
    Bormans, Concetta
    Marcu, Shai
    Tayeb-Fligelman, Einav
    Vinkler, Chana
    Raas-Rothschild, Annick
    Irge, Dana
    Landau, Meytal
    Shohat, Mordechai
    Puente, Xose S.
    Behar, Doron M.
    Lopez-Otin, Carlos
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2016, 24 (12) : 1792 - 1796
  • [24] Biallelic mutations in NRROS cause an early onset lethal microgliopathy
    Smith, Colin
    McColl, Barry W.
    Patir, Anirudh
    Barrington, Jack
    Armishaw, Jeremy
    Clarke, Antonia
    Eaton, Jenny
    Hobbs, Vivienne
    Mansour, Sahar
    Nolan, Melinda
    Rice, Gillian I.
    Rodero, Mathieu P.
    Seabra, Luis
    Uggenti, Carolina
    Livingston, John H.
    Bridges, Leslie R.
    Jeffrey, Iona J. M.
    Crow, Yanick J.
    ACTA NEUROPATHOLOGICA, 2020, 139 (05) : 947 - 951
  • [25] Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
    Efthymiou, S.
    Salpietro, V.
    Malintan, N.
    Poncelet, M.
    Kriouile, Y.
    Fortuna, S.
    de Zorzi, R.
    Payne, K.
    Henderson, L.
    Cortese, A.
    Maddirevula, S.
    Alhashmi, N.
    Wiethoff, S.
    Ryten, M.
    Botia, J.
    Provitera, V.
    Schuelke, M.
    Vandrovcova, J.
    Walsh, L.
    Torti, E.
    Iodice, V.
    Najafi, M.
    Karimiani, E.
    Maroofian, R.
    Siquier-Pernet, K.
    Boddaert, N.
    De Lonlay, P.
    Cantagrel, V.
    Aguennouz, M.
    El Khorassani, M.
    Schmidts, M.
    Alkuraya, F. S.
    Edvardson, S.
    Nolano, M.
    Devaux, J.
    Houlden, H.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 438 - 439
  • [26] Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
    Efthymiou, Stephanie
    Salpietro, Vincenzo
    Malintan, Nancy
    Poncelet, Mallory
    Kriouile, Yamna
    Fortuna, Sara
    De Zorzi, Rita
    Payne, Katelyn
    Henderson, Lindsay B.
    Cortese, Andrea
    Maddirevula, Sateesh
    Alhashmi, Nadia
    Wiethoff, Sarah
    Ryten, Mina
    Botia, Juan A.
    Provitera, Vincenzo
    Schuelke, Markus
    Vandrovcova, Jana
    Groppa, Stanislav
    Karashova, Blagovesta Marinova
    Nachbauer, Wolfgang
    Boesch, Sylvia
    Arning, Larissa
    Timmann, Dagmar
    Cormand, Bru
    Perez-Duenas, Belen
    Goraya, Jatinder S.
    Sultan, Tipu
    Mine, Jun
    Avdjieva, Daniela
    Kathom, Hadil
    Tincheva, Radka
    Banu, Selina
    Pineda-Marfa, Mercedes
    Veggiotti, Pierangelo
    Ferrari, Michel D.
    van den Maagdenberg, Arn M. J. M.
    Verrotti, Alberto
    Marseglia, Giangluigi
    Savasta, Salvatore
    Garcia-Silva, Mayte
    Ruiz, Alfons Macaya
    Garavaglia, Barbara
    Borgione, Eugenia
    Portaro, Simona
    Sanchez, Benigno Monteagudo
    Boles, Richard
    Papacostas, Savvas
    Vikelis, Michail
    Rothman, James
    BRAIN, 2019, 142 : 2948 - 2964
  • [27] Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C
    Eyal Reinstein
    Ana Gutierrez-Fernandez
    Shay Tzur
    Concetta Bormans
    Shai Marcu
    Einav Tayeb-Fligelman
    Chana Vinkler
    Annick Raas-Rothschild
    Dana Irge
    Meytal Landau
    Mordechai Shohat
    Xose S Puente
    Doron M Behar
    Carlos Lopez-Otın
    European Journal of Human Genetics, 2016, 24 : 1792 - 1796
  • [28] Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
    Jun Shen
    Edward C Gilmore
    Christine A Marshall
    Mary Haddadin
    John J Reynolds
    Wafaa Eyaid
    Adria Bodell
    Brenda Barry
    Danielle Gleason
    Kathryn Allen
    Vijay S Ganesh
    Bernard S Chang
    Arthur Grix
    R Sean Hill
    Meral Topcu
    Keith W Caldecott
    A James Barkovich
    Christopher A Walsh
    Nature Genetics, 2010, 42 : 245 - 249
  • [29] Biallelic mutations in NRROS cause an early onset lethal microgliopathy
    Colin Smith
    Barry W. McColl
    Anirudh Patir
    Jack Barrington
    Jeremy Armishaw
    Antonia Clarke
    Jenny Eaton
    Vivienne Hobbs
    Sahar Mansour
    Melinda Nolan
    Gillian I. Rice
    Mathieu P. Rodero
    Luis Seabra
    Carolina Uggenti
    John H. Livingston
    Leslie R. Bridges
    Iona J. M. Jeffrey
    Yanick J. Crow
    Acta Neuropathologica, 2020, 139 : 947 - 951
  • [30] RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans
    Shamseldin, Hanan
    Alazami, Anas M.
    Manning, Melanie
    Hashem, Amal
    Caluseiu, Oana
    Tabarki, Brahim
    Esplin, Edward
    Schelley, Susan
    Innes, A. Micheil
    Parboosingh, Jillian S.
    Lamont, Ryan
    Majewski, Jacek
    Bernier, Francois P.
    Alkuraya, Fowzan S.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 97 (06) : 862 - 868