Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

X linked congenital stationary night blindness (CSNBX) is a non-progressive retinal disorder characterised by decreased visual acuity and disturbance of night vision. CSNBX appears to be not only clinically but also genetically heterogeneous. On studying a single large family, we recently suggested...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Bergen, A A, ten Brink, J B, Riemslag, F, Schuurman, E J, Meire, F, Tijmes, N, de Jong, P T
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1996
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050769/
https://ncbi.nlm.nih.gov/pubmed/8933343
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