A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3.

Congenital nystagmus (CN) is a common oculomotor disorder (frequency of 1/1,500 live births) characterized by bilateral uncontrollable ocular oscillations, with onset typically at birth or within the first few months of life. This condition is regarded as idiopathic, after exclusion of nervous and o...

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Detalhes bibliográficos
Main Authors: Cabot, A, Rozet, J M, Gerber, S, Perrault, I, Ducroq, D, Smahi, A, Souied, E, Munnich, A, Kaplan, J
Formato: Artigo
Idioma:Inglês
Publicado em: 1999
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377838/
https://ncbi.nlm.nih.gov/pubmed/10090899
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