Syndromic inherited poikiloderma due to a de novo mutation in FAM111B.

Takeichi, T; Nanda, A; Yang, H-S; Hsu, C-K; Lee, J Y-Y; Al-Ajmi, H; Akiyama, M; Simpson, M A; McGrath, J A

Takeichi, T; Nanda, A; Yang, H-S; Hsu, C-K; Lee, J Y-Y; Al-Ajmi, H; Akiyama, M; Simpson, M A; McGrath, J A.

Afiliación

Takeichi T; St John's Institute of Dermatology, King's College London, Guy's Hospital, London, U.K.
Nanda A; Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yang HS; As'ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait.
Hsu CK; Department of Dermatology, National Cheng Kung University Hospital, National Cheng Kung University, Tainan, Taiwan.
Lee JY; Department of Dermatology, National Cheng Kung University Hospital, National Cheng Kung University, Tainan, Taiwan.
Al-Ajmi H; Institute of Clinical Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Akiyama M; Department of Dermatology, National Cheng Kung University Hospital, National Cheng Kung University, Tainan, Taiwan.
Simpson MA; As'ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait.
McGrath JA; Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Br J Dermatol ; 176(2): 534-536, 2017 02.

Article en En | MEDLINE | ID: mdl-27406236

Asunto(s)

Proteínas de Ciclo Celular/genética; Contractura/genética; Mutación Missense/genética; Fibrosis Pulmonar/genética; Esclerosis/genética; Anomalías Cutáneas/genética; Enfermedades Cutáneas Genéticas/genética; Adolescente; Femenino; Humanos; Síndrome

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Pulmonar / Esclerosis / Anomalías Cutáneas / Enfermedades Cutáneas Genéticas / Proteínas de Ciclo Celular / Contractura / Mutación Missense Límite: Adolescent / Female / Humans Idioma: En Revista: Br J Dermatol Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

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