Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: NUDT2[original query] |
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Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield. Molecular psychiatry 2016 Jul . Anazi S, Maddirevula S, Faqeih E, Alsedairy H, Alzahrani F, Shamseldin H E, Patel N, Hashem M, Ibrahim N, Abdulwahab F, Ewida N, Alsaif H S, Al Sharif H, Alamoudi W, Kentab A, Bashiri F A, Alnaser M, AlWadei A H, Alfadhel M, Eyaid W, Hashem A, Al Asmari A, Saleh M M, AlSaman A, Alhasan K A, Alsughayir M, Al Shammari M, Mahmoud A, Al-Hassnan Z N, Al-Husain M, Osama Khalil R, Abd El Meguid N, Masri A, Ali R, Ben-Omran T, El Fishway P, Hashish A, Ercan Sencicek A, State M, Alazami A M, Salih M A, Altassan N, Arold S T, Abouelhoda M, Wakil S M, Monies D, Shaheen R, Alkuraya F |
The first case of intellectual disability caused by novel compound heterozygosity for NUDT2 variants. BMC pediatrics 2024 1 24 (1): 60. Bo Bi, Xiaohong Chen, Shan Huang, Min Peng, Weiyue Gu, Hongmin Zhu, Yangcan Mi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
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