Your browser doesn't support javascript.
loading
De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.
Sakamoto, Masamune; Sasaki, Kazunori; Sugie, Atsushi; Nitta, Yohei; Kimura, Tetsuaki; Gürsoy, Semra; Cinleti, Tayfun; Iai, Mizue; Sengoku, Toru; Ogata, Kazuhiro; Suzuki, Atsushi; Okamoto, Nobuhiko; Iwama, Kazuhiro; Tsuchida, Naomi; Uchiyama, Yuri; Koshimizu, Eriko; Fujita, Atsushi; Hamanaka, Kohei; Miyatake, Satoko; Mizuguchi, Takeshi; Taguri, Masataka; Ito, Shuuichi; Takahashi, Hidehisa; Miyake, Noriko; Matsumoto, Naomichi.
Afiliación
  • Sakamoto M; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Sasaki K; Department of Pediatrics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Sugie A; Department of Molecular Biology, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Nitta Y; Department of Cancer Biology, Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
  • Kimura T; Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
  • Gürsoy S; Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
  • Cinleti T; Division of Human Genetics, Department of Integrated Genetics, National Institute of Genetics, Mishima, 411-8540, Japan.
  • Iai M; Department of Pediatric Genetics, S.B.Ü. Dr. Behçet Uz Children's Education and Research Hospital, Izmir, 35210, Turkey.
  • Sengoku T; Department of Pediatric Genetics, Dokuz Eylul University, Faculty of Medicine, Izmir, 35340, Turkey.
  • Ogata K; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, 232-8555, Japan.
  • Suzuki A; Department of Biochemistry, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Okamoto N; Department of Biochemistry, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Iwama K; Molecular Cellular Biology Laboratory, Yokohama City University Graduate School of Medical Life Science, Yokohama, 230-0045, Japan.
  • Tsuchida N; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, 594-1101, Japan.
  • Uchiyama Y; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Koshimizu E; Department of Pediatrics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Fujita A; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Hamanaka K; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, 236-0004, Japan.
  • Miyatake S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Mizuguchi T; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, 236-0004, Japan.
  • Taguri M; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Ito S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Takahashi H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Miyake N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
  • Matsumoto N; Clinical Genetics Department, Yokohama City University Hospital, Yokohama, 236-0004, Japan.
Hum Mol Genet ; 31(1): 69-81, 2021 12 17.
Article en En | MEDLINE | ID: mdl-34346499
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factores de Ribosilacion-ADP / Trastornos del Neurodesarrollo Límite: Animals Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factores de Ribosilacion-ADP / Trastornos del Neurodesarrollo Límite: Animals Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Japón