Your browser doesn't support javascript.
loading
A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology.
Okamoto, Nobuhiko; Tsuchiya, Yuki; Miya, Fuyuki; Tsunoda, Tatsuhiko; Yamashita, Kumiko; Boroevich, Keith A; Kato, Mitsuhiro; Saitoh, Shinji; Yamasaki, Mami; Kanemura, Yonehiro; Kosaki, Kenjiro; Kitagawa, Daiju.
Afiliação
  • Okamoto N; Department of Medical Genetics, Osaka Women's and Children's Hospital, Izumi, Osaka, Japan.
  • Tsuchiya Y; Department of Molecular Medicine, Osaka Women's and Children's Hospital, Izumi, Osaka, Japan.
  • Miya F; National Institute of Genetics, Department of Molecular Genetics, Division of Centrosome Biology, Mishima, Shizuoka, Japan.
  • Tsunoda T; Department of Genetics, School of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka, Japan.
  • Yamashita K; Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
  • Boroevich KA; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Kato M; Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
  • Saitoh S; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Yamasaki M; Biwako Gakuen Kusatsu Medical and Welfare Center for Children and Persons with Severe Motor and Intellectual Disabilities, Kusatsu, Japan.
  • Kanemura Y; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Kosaki K; Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan.
  • Kitagawa D; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Am J Med Genet A ; 173(10): 2690-2696, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28777490
Assuntos
Palavras-chave
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Mutação da Fase de Leitura / Deficiência Intelectual / Mitose / Fuso Acromático Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Mutação da Fase de Leitura / Deficiência Intelectual / Mitose / Fuso Acromático Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão País de publicação: Estados Unidos