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Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Alder, Jonathan K; Stanley, Susan E; Wagner, Christa L; Hamilton, Makenzie; Hanumanthu, Vidya Sagar; Armanios, Mary.
Afiliação
  • Alder JK; Department of Oncology and Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT.
  • Stanley SE; Department of Oncology and Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Wagner CL; Department of Oncology and Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Hamilton M; Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT.
  • Hanumanthu VS; Department of Oncology and Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Armanios M; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD. Electronic address: marmani1@jhmi.edu.
Chest ; 147(5): 1361-1368, 2015 May.
Article em En | MEDLINE | ID: mdl-25539146
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar / Deleção de Sequência / Mutação de Sentido Incorreto / Proteínas de Ligação a Telômeros / Exoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Chest Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar / Deleção de Sequência / Mutação de Sentido Incorreto / Proteínas de Ligação a Telômeros / Exoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Chest Ano de publicação: 2015 Tipo de documento: Article