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Mutations in NMNAT1 cause Leber congenital amaurosis with severe macular and optic atrophy

scientific article

Author/s

author: Jean-michel Rozet, Josseline Kaplan, Isabelle Perrault, Hélène Dollfus, Sylvain Hanein

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Work details

Publication date
January 25, 2013
- -
Language
French

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