Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype.
Academic Article
Publication Date:
2007
CRIS type:
1.1 Articolo in rivista
List of contributors:
Perrault, I; Delphin, N; Hanein, S; Gerber, S; Dufier, Jl; Roche, O; DEFOORT DHELLEMMES, S; Dollfus, H; Fazzi, Elisa Maria; Munnich, A; Kaplan, J; Rozet, Jm
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