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A case of PAPASH syndrome in a young man carrying a novel heterozygote missense variant in PSTPIP1.
Kotzerke, M; Mitri, F; Marbach, F; Enk, A; Haenssle, H.
Affiliation
  • Kotzerke M; Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
  • Mitri F; Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
  • Marbach F; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.
  • Enk A; Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
  • Haenssle H; Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
J Eur Acad Dermatol Venereol ; 35(7): e439-e440, 2021 Jul.
Article in En | MEDLINE | ID: mdl-33587775
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyoderma Gangrenosum / Mutation, Missense Limits: Humans / Male Language: En Journal: J Eur Acad Dermatol Venereol Journal subject: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Year: 2021 Document type: Article Affiliation country: Germany
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyoderma Gangrenosum / Mutation, Missense Limits: Humans / Male Language: En Journal: J Eur Acad Dermatol Venereol Journal subject: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Year: 2021 Document type: Article Affiliation country: Germany