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Novel SLC20A2 mutation in a Japanese pedigree with primary familial brain calcification.
Kuroi, Yasuhiro; Akagawa, Hiroyuki; Yoneyama, Taku; Kikuchi, Asami; Maegawa, Tatsuya; Onda, Hideaki; Kasuya, Hidetoshi.
Afiliación
  • Kuroi Y; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
  • Akagawa H; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan; Tokyo Women's Medical University Institute for Integrated Medical Sciences (TIIMS), Tokyo, Japan. Electronic address: akagawa.hiroyuki@twmu.ac.jp.
  • Yoneyama T; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
  • Kikuchi A; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
  • Maegawa T; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
  • Onda H; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan; Division of Neurosurgery, Kofu Neurosurgical Hospital, Kofu, Yamanashi, Japan.
  • Kasuya H; Department of Neurosurgery, Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
J Neurol Sci ; 399: 183-185, 2019 04 15.
Article en En | MEDLINE | ID: mdl-30826713
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Encefalopatías / Calcinosis / Proteínas Cotransportadoras de Sodio-Fosfato de Tipo III / Mutación Límite: Aged / Female / Humans País/Región como asunto: Asia Idioma: En Revista: J Neurol Sci Año: 2019 Tipo del documento: Article País de afiliación: Japón
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Encefalopatías / Calcinosis / Proteínas Cotransportadoras de Sodio-Fosfato de Tipo III / Mutación Límite: Aged / Female / Humans País/Región como asunto: Asia Idioma: En Revista: J Neurol Sci Año: 2019 Tipo del documento: Article País de afiliación: Japón