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Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.
Almuriekhi, Mariam; Shintani, Takafumi; Fahiminiya, Somayyeh; Fujikawa, Akihiro; Kuboyama, Kazuya; Takeuchi, Yasushi; Nawaz, Zafar; Nadaf, Javad; Kamel, Hussein; Kitam, Abu Khadija; Samiha, Zaineddin; Mahmoud, Laila; Ben-Omran, Tawfeg; Majewski, Jacek; Noda, Masaharu.
Afiliação
  • Almuriekhi M; Section of Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Shintani T; Division of Molecular Neurobiology, National Institute for Basic Biology, Okazaki 444-8787, Japan; School of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Okazaki 444-8787, Japan.
  • Fahiminiya S; Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, QC H3A 1B1, Canada; McGill University and Génome Québec Innovation Centre, Montreal, QC H3A 0G1, Canada.
  • Fujikawa A; Division of Molecular Neurobiology, National Institute for Basic Biology, Okazaki 444-8787, Japan.
  • Kuboyama K; Division of Molecular Neurobiology, National Institute for Basic Biology, Okazaki 444-8787, Japan.
  • Takeuchi Y; Division of Molecular Neurobiology, National Institute for Basic Biology, Okazaki 444-8787, Japan.
  • Nawaz Z; Cytogenetic and Molecular Cytogenetic Laboratory, Department of Laboratory Medicine and Pathology, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Nadaf J; Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, QC H3A 1B1, Canada; McGill University and Génome Québec Innovation Centre, Montreal, QC H3A 0G1, Canada.
  • Kamel H; Department of Radiology, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Kitam AK; Cytogenetic and Molecular Cytogenetic Laboratory, Department of Laboratory Medicine and Pathology, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Samiha Z; Cytogenetic and Molecular Cytogenetic Laboratory, Department of Laboratory Medicine and Pathology, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Mahmoud L; Section of Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Ben-Omran T; Section of Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
  • Majewski J; Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, QC H3A 1B1, Canada; McGill University and Génome Québec Innovation Centre, Montreal, QC H3A 0G1, Canada.
  • Noda M; Division of Molecular Neurobiology, National Institute for Basic Biology, Okazaki 444-8787, Japan; School of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Okazaki 444-8787, Japan. Electronic address: madon@nibb.ac.jp.
Cell Rep ; 10(9): 1585-1598, 2015 Mar 10.
Article em En | MEDLINE | ID: mdl-25753423
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article