Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 30 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. FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus;Genes;2023-01-29
2. Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia;European Journal of Human Genetics;2022-10-07
3. The challenges faced by clinicians diagnosing and treating infantile nystagmus Part I: diagnosis;Expert Review of Ophthalmology;2020-12-17
4. p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus;Frontiers in Cell and Developmental Biology;2020-11-04
5. Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families;Human Genetics;2020-04-04
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