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Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.
Vona, Barbara; Müller, Tobias; Nanda, Indrajit; Neuner, Cordula; Hofrichter, Michaela A H; Schröder, Jörg; Bartsch, Oliver; Läßig, Anne; Keilmann, Annerose; Schraven, Sebastian; Kraus, Fabian; Shehata-Dieler, Wafaa; Haaf, Thomas.
Afiliação
  • Vona B; Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Müller T; Department of Bioinformatics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Nanda I; Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Neuner C; Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Hofrichter MA; Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Schröder J; Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Bartsch O; Institute of Human Genetics, University Medical Centre, Johannes Gutenberg University, Mainz, Germany.
  • Läßig A; Division of Communication Disorders, Department of Otorhinolaryngology, University Medical Centre, Johannes Gutenberg University, Mainz, Germany.
  • Keilmann A; Division of Communication Disorders, Department of Otorhinolaryngology, University Medical Centre, Johannes Gutenberg University, Mainz, Germany.
  • Schraven S; Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, Comprehensive Hearing Center, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Kraus F; Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, Comprehensive Hearing Center, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Shehata-Dieler W; Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, Comprehensive Hearing Center, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
  • Haaf T; Institute of Human Genetics, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
Genet Med ; 16(12): 945-53, 2014 Dec.
Article em En | MEDLINE | ID: mdl-24875298
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article