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Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT.

Takuya TakeichiK SugiuraK TanahashiK NodaMichihiro KonoM Akiyama
Published in: The British journal of dermatology (2018)
Keyphrases
  • multiple sclerosis
  • intellectual disability