Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

2012 | journal article

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​Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin​
Huppke, P.; Brendel, C.; Kalscheuer, V.; Korenke, G.; Marquardt, I.; Freisinger, P. & Christodoulou, J. et al.​ (2012) 
The American Journal of Human Genetics90(2) pp. 378​.​ DOI: https://doi.org/10.1016/j.ajhg.2012.01.015 

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Authors
Huppke, Peter; Brendel, Cornelia; Kalscheuer, Vera; Korenke, Georg Christoph; Marquardt, Iris; Freisinger, Peter; Christodoulou, John; Hillebrand, Merle; Pitelet, Gaele; Wilson, Callum; Gärtner, Jutta 
Issue Date
2012
Journal
The American Journal of Human Genetics 
ISSN
0002-9297
Language
English

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