Wikidata

(Q46901354)

English

Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II.

scientific article published in December 2007

In more languages

Statements

title
Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18000884
retrieved
26 December 2017
reference URL
http://europepmc.org/abstract/MED/18000884

Identifiers

 
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