Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin
- 1 January 2012
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 90 (1), 61-68
- https://doi.org/10.1016/j.ajhg.2011.11.030
Abstract
No abstract availableKeywords
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