Aplasia of cochlear nerves and olfactory bulbs in association withSOX10mutation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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3. Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10;Bondurand;Hum Mol Genet,2001
4. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4;Bondurand;Am J Hum Genet,2007
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