A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene;Stem Cell Research;2024-09
2. INTS11-related neurodevelopmental disorder: a case report and literature review;Journal of Human Genetics;2024-07-19
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