Wolfram gene (WFS1) mutation causes autosomal dominant...

European Journal of Human Genetics 2013 / 12 Vol. 21; Iss. 12

Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans

Berry, Vanita, Gregory-Evans, Cheryl, Emmett, Warren, Waseem, Naushin, Raby, Jacob, Prescott, DeQuincy, Moore, Anthony T, Bhattacharya, Shomi S
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Volume:
21
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2013.52
Date:
December, 2013
File:
PDF, 1.19 MB
english, 2013
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