Your browser doesn't support javascript.
loading
Malta (MYH9 Associated Elastin Aggregation) Syndrome: Germline Variants in MYH9 Cause Rare Sweat Duct Proliferations and Irregular Elastin Aggregations.
Fewings, Eleanor; Ziemer, Mirjana; Hörtnagel, Konstanze; Reicherter, Kerstin; Larionov, Alexey; Redman, James; Goldgraben, Mae A; Pepler, Alexander; Hearn, Tim; Firth, Helen; Ha, Tom; Schaller, Jörg; Adams, David J; Rytina, Ed; van Steensel, Maurice; Tischkowitz, Marc.
Afiliação
  • Fewings E; Academic Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.
  • Ziemer M; Department of Dermatology, Venerology and Allergology, University of Leipzig Medical Center, Leipzig, Germany.
  • Hörtnagel K; Center for Genomics and Transcriptomics and Praxis für Humangenetik Tübingen, Tübingen, Germany.
  • Reicherter K; Center for Genomics and Transcriptomics and Praxis für Humangenetik Tübingen, Tübingen, Germany.
  • Larionov A; Academic Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.
  • Redman J; Academic Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.
  • Goldgraben MA; Academic Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.
  • Pepler A; Center for Genomics and Transcriptomics and Praxis für Humangenetik Tübingen, Tübingen, Germany.
  • Hearn T; Academic Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom.
  • Firth H; East Anglian Medical Genetics Service, Cambridge University Hospitals National Health Service Foundation Trust, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • Ha T; Department of Dermatology, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • Schaller J; Dermatopathologie Duisburg, Duisburg, Germany.
  • Adams DJ; Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, United Kingdom.
  • Rytina E; Department of Histopathology, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • van Steensel M; Skin Research Institute of Singapore, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore; Lee Kong Chian Medical School, Nanyang Technological University, Singapore, Singapore.
  • Tischkowitz M; Academic Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom; East Anglian Medical Genetics Service, Cambridge University Hospitals National Health Service Foundation Trust, Cambridge Biomedical Campus, Cambridge, United Kingdom. Electronic address: mdt33@medschl.cam.a
J Invest Dermatol ; 139(10): 2238-2241.e6, 2019 10.
Article em En | MEDLINE | ID: mdl-31125547
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glândulas Sudoríparas / Trombocitopenia / Transtornos Plaquetários / Agregação Plaquetária / Cadeias Pesadas de Miosina / Predisposição Genética para Doença / Perda Auditiva Neurossensorial Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glândulas Sudoríparas / Trombocitopenia / Transtornos Plaquetários / Agregação Plaquetária / Cadeias Pesadas de Miosina / Predisposição Genética para Doença / Perda Auditiva Neurossensorial Idioma: En Ano de publicação: 2019 Tipo de documento: Article