Leber Congenital Amaurosis: Comprehensive Survey of the Genetic Heterogeneity, Refinement of the Clinical Definition, and Genotype-Phenotype Correlations as a Strategy for Molecular Diagnosis

AuthID
 P-000-CVN
18
Author(s)
Gerber, S
·
Tanguy, G
·
Barbet, F
·
Ducroq, D
·
Calvas, P
·
Hamel, C
·
Lopponen, T
·
Munier, F
·
Santos, L
·
Shalev, S
·
Rozet, JM
·
Kaplan, J
Document Type
Article
Year published
2004
Published
in HUMAN MUTATION, ISSN: 1059-7794
Volume: 23, Issue: 4, Pages: 306-317 (12)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 15024725
Scopus: 2-s2.0-11144356431
Wos: WOS:000220471700003
Source Identifiers
ISSN: 1059-7794
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