Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport
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- 1 June 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (6), 1359-1369
- https://doi.org/10.1086/375454
Abstract
No abstract availableKeywords
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