Your browser doesn't support javascript.
loading
Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people.
Yamamoto, Ken; Ishii, Eiichi; Horiuchi, Hisanori; Ueda, Ikuyo; Ohga, Shouichi; Nishi, Masanori; Ogata, Yoshiyasu; Zaitsu, Masafumi; Morimoto, Akira; Hara, Toshiro; Imashuku, Shinsaku; Sasazuki, Takehiko; Yasukawa, Masaki.
Afiliación
  • Yamamoto K; Department of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Ishii E; Department of Pediatrics, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan. ishiei@med.saga-u.ac.jp.
  • Horiuchi H; Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Ueda I; Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Ohga S; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Nishi M; Department of Pediatrics, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan.
  • Ogata Y; Department of Pediatrics, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan.
  • Zaitsu M; Department of Pediatrics, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga, 849-8501, Japan.
  • Morimoto A; Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Hara T; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Imashuku S; Division of Pediatrics, Takasago Seibu Hospital, Takasago, Japan.
  • Sasazuki T; Research Institute, International Medical Center of Japan, Tokyo, Japan.
  • Yasukawa M; First Department of Internal Medicine, Ehime University, Ehime, Japan.
J Hum Genet ; 50(11): 600-603, 2005.
Article en En | MEDLINE | ID: mdl-16180048
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Linfohistiocitosis Hemofagocítica / Proteínas Qa-SNARE / Proteínas Qb-SNARE / Proteínas Qc-SNARE Tipo de estudio: Etiology_studies Límite: Female / Humans / Infant / Male País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2005 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Linfohistiocitosis Hemofagocítica / Proteínas Qa-SNARE / Proteínas Qb-SNARE / Proteínas Qc-SNARE Tipo de estudio: Etiology_studies Límite: Female / Humans / Infant / Male País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2005 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido