Identification and functional analysis of SOX10 phosphorylation sites in melanoma
Author:
Funder
National Human Genome Research Institute
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference79 articles.
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3. Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation;K Inoue;Ann Neurol,1999
4. Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain (vol 66, pg 1496, 2000);Touraine;American Journal of Human Genetics,2000
5. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4;N Bondurand;American Journal of Human Genetics,2007
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