Mutations in Nmnat1 Cause Leber Congenital Amaurosis with Early-Onset Severe Macular and Optic Atrophy

AuthID
 P-002-674
23
Author(s)
Serre, V
·
Nicouleau, M
·
Fares Taie, L
·
[+1]·
[+1]·
[+1]·
Nitschke, P
·
Calvas, P
·
Roche, O
·
Kaplan, J
·
Rozet, JM
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Document Type
Article
Year published
2012
Published
in NATURE GENETICS, ISSN: 1061-4036
Volume: 44, Issue: 9, Pages: 975-977 (3)
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Scopus®
Crossref®64
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 22842229
Scopus: 2-s2.0-84865680230
Wos: WOS:000308491200007
Source Identifiers
ISSN: 1061-4036
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All authors
Name Order Nome   Name Order Nome   Name Order Nome
1 Perrault, I;   2 Hanein, S;   3 Zanlonghi, X;
4 Serre, V;   5 Nicouleau, M;   6 Defoort Delhemmes, S;
7 Delphin, N;   8 Fares Taie, L;   9 Gerber, S;
10 Xerri, O;   11 Edelson, C;   12 Goldenberg, A;
13 Duncombe, A;   14 Le Meur, G;   15 Hamel, C;
16 Silva, E ;   17 Nitschke, P;   18 Calvas, P;
19 Munnich, A;   20 Roche, O;   21 Dollfus, H;
22 Kaplan, J;   23 Rozet, JM;  

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