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Japanese case of Mal de Meleda with a novel missense mutation of p.Thr52Ala in the second protruding finger of secreted Ly-6/uPAR-related protein 1.

Makoto KunisadaKiyofumi YamanishiChikako Nishigori
Published in: The Journal of dermatology (2019)
Keyphrases
  • intellectual disability