A Crx Null Mutation Is Associated with Both Leber Congenital Amaurosis and a Normal Ocular Phenotype

AuthID
 P-008-TWE
6
Author(s)
Yang, JM
·
Li, Y
·
Dharmaraj, S
·
Sundin, OH
·
Maumenee, IH
Tipo de Documento
Article
Year published
2000
Publicado
in Investigative Ophthalmology and Visual Science, ISSN: 0146-0404
Volume: 41, Número: 8, Páginas: 2076-2079
Indexing
Scopus®
Pubmed®
Publication Identifiers
Pubmed: 10892846
SCOPUS: 2-s2.0-0033949797
Source Identifiers
ISSN: 0146-0404
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