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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

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Description scientific article
Author/s

author: Hui Wang  James A Poulter  Jeremy Schwartzentruber  Chris F. Inglehearn  Carmel Toomes  Jacek Majewski  Robert Koenekoop  Clare Victoria Logan  David Parry  Xia Wang 

Publication date September 2012
Language English
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