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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Cabot, A, Rozet, J M, Gerber, S, Perrault, I, Ducroq, D, Smahi, A, Souied, E, Munnich, A, Kaplan, J
Médium: Artigo
Jazyk:Inglês
Vydáno: 1999
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377838/
https://ncbi.nlm.nih.gov/pubmed/10090899
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky