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Familial hypotrichosis simplex of the scalp associated with a novel heterozygous nonsense variant in CDSN.
Rayinda, Tuntas; McSweeney, Sheila M; Lalagianni, Nikolina; Liu, Lu; Guy, Alyson; Fenton, David; Stefanato, Catherine M; Dand, Nick; McGrath, John A; Tziotzios, Christos.
Afiliação
  • Rayinda T; St John's Institute of Dermatology, King's College London, UK.
  • McSweeney SM; Department of Dermatology and Venereology, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Indonesia.
  • Lalagianni N; St John's Institute of Dermatology, King's College London, UK.
  • Liu L; St John's Institute of Dermatology, King's College London, UK.
  • Guy A; Viapath, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Fenton D; Viapath, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Stefanato CM; St John's Institute of Dermatology, King's College London, UK.
  • Dand N; St John's Institute of Dermatology, King's College London, UK.
  • McGrath JA; Department of Medical and Molecular Genetics, King's College London, UK.
  • Tziotzios C; St John's Institute of Dermatology, King's College London, UK.
Clin Exp Dermatol ; 48(5): 579-583, 2023 04 27.
Article em En | MEDLINE | ID: mdl-36864587
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Couro Cabeludo / Hipotricose Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Couro Cabeludo / Hipotricose Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article