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SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome.

Hirohito ShimaEtsuro TokuhiroShingo OkamotoMariko NagamoriTsutomu OgataSatoshi NarumiAkie NakamuraYoko IzumiTomoko JinnoErina SuzukiMaki Fukami
Published in: Journal of the Endocrine Society (2021)
These results provide evidence that SOX10 haploinsufficiency accounts for a small percentage of KS cases. SOX10 haploinsufficiency is likely to be associated with a broad phenotypic spectrum, which includes KS without other clinical features of WS/PCWH.
Keyphrases
  • transcription factor
  • stem cells