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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Bibliografske podrobnosti
Main Authors: Cabot, A, Rozet, J M, Gerber, S, Perrault, I, Ducroq, D, Smahi, A, Souied, E, Munnich, A, Kaplan, J
Format: Artigo
Jezik:Inglês
Izdano: 1999
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377838/
https://ncbi.nlm.nih.gov/pubmed/10090899
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