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Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin
scientific article
Author/s
author: Vera M. Kalscheuer, Gudrun Nürnberg, Lisbeth Birk Møller, John Christodoulou, Stefan Haas, Peter Nürnberg, Peter Huppke
Work details
Publication date
January 1, 2012
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Language
English
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