Additive dominant effect of a SOX10 mutation underlies a complex phenotype of PCWH-Reference-Cited by-同舟云学术

Additive dominant effect of a SOX10 mutation underlies a complex phenotype of PCWH

Published:2015-08 Issue: Volume:80 Page:1-14
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Ito Yukiko,Inoue Naoko,Inoue Yukiko U.,Nakamura Shoko,Matsuda Yoshiki,Inagaki Masumi,Ohkubo Takahiro,Asami Junko,Terakawa Youhei W.,Kohsaka Shinichi,Goto Yu-ichi,Akazawa Chihiro,Inoue Takayoshi,Inoue Ken

Publisher

Elsevier BV

Subject

Neurology

Reference47 articles.

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2. The role of SOX10 during enteric nervous system development;Bondurand;Dev. Biol.,2013

3. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4;Bondurand;Am. J. Hum. Genet.,2007

4. Sox10 is required for Schwann-cell homeostasis and myelin maintenance in the adult peripheral nerve;Bremer;Glia,2011

5. The transcription factor Sox10 is a key regulator of peripheral glial development;Britsch;Genes Dev.,2001

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