Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference36 articles.
1. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies
2. Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3 - 8q22.1: Redefining a clinical entity
3. Refined Mapping of the Cohen Syndrome Gene by Linkage Disequilibrium
4. 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
5. Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants ofCOH1
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