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Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect.
Edelbusch, Christine; Cindric, Sandra; Dougherty, Gerard W; Loges, Niki T; Olbrich, Heike; Rivlin, Joseph; Wallmeier, Julia; Pennekamp, Petra; Amirav, Israel; Omran, Heymut.
Afiliação
  • Edelbusch C; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Cindric S; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Dougherty GW; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Loges NT; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Olbrich H; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Rivlin J; Department of Pediatrics, Carmel Medical Center, Haifa, Israel.
  • Wallmeier J; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Pennekamp P; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
  • Amirav I; Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
  • Omran H; Department of General Pediatrics, University Children's Hospital Muenster, Muenster, Germany.
Hum Mutat ; 38(8): 964-969, 2017 08.
Article em En | MEDLINE | ID: mdl-28543983
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Motilidade Ciliar / Proteínas Serina-Treonina Quinases / Mutação Tipo de estudo: Etiology_studies Limite: Female / Humans / Male Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos da Motilidade Ciliar / Proteínas Serina-Treonina Quinases / Mutação Tipo de estudo: Etiology_studies Limite: Female / Humans / Male Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha