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Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia.
Bonczek, Ondrej; Bielik, Peter; Krejcí, Premysl; Zeman, Tomás; Izakovicová-Hollá, Lýdie; Soukalová, Jana; Vanek, Jirí; Gerguri, Tereza; Balcar, Vladimir J; Serý, Omar.
Afiliação
  • Bonczek O; Laboratory of Neurobiology and Molecular Psychiatry, Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic.
  • Bielik P; Laboratory of Neurobiology and Pathological Physiology, Institute of Animal Physiology and Genetics, The Academy of Sciences of the Czech Republic, Brno, Czech Republic.
  • Krejcí P; Laboratory of Neurobiology and Molecular Psychiatry, Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic.
  • Zeman T; Institute of Dentistry and Oral Sciences, Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic.
  • Izakovicová-Hollá L; Laboratory of Neurobiology and Molecular Psychiatry, Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic.
  • Soukalová J; Clinic of Stomatology, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
  • Vanek J; Clinic of Stomatology, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
  • Gerguri T; Clinic of Stomatology, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
  • Balcar VJ; Biomolecular Modelling Laboratory, The Francis Crick Institute, London, United Kingdom.
  • Serý O; Laboratory of Neurobiology and Pathological Physiology, Institute of Animal Physiology and Genetics, The Academy of Sciences of the Czech Republic, Brno, Czech Republic.
PLoS One ; 13(9): e0202989, 2018.
Article em En | MEDLINE | ID: mdl-30192788
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Códon sem Sentido / Fator de Transcrição MSX1 / Anodontia Tipo de estudo: Prognostic_studies Limite: Adolescent / Female / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: República Tcheca
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Códon sem Sentido / Fator de Transcrição MSX1 / Anodontia Tipo de estudo: Prognostic_studies Limite: Adolescent / Female / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: República Tcheca