Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0534.

Vallespin, E

Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0534. [electronic resource] - Human genetics Feb 2006 - 777 p. digital

Publication Type: Journal Article

0340-6717


Amino Acid Substitution
Eye Proteins--genetics
Humans
Membrane Proteins--genetics
Mutation, Missense
Nerve Tissue Proteins--genetics
Optic Atrophy, Hereditary, Leber--genetics