Your browser doesn't support javascript.
loading
Biochemical and molecular characterisation of neurological Wilson disease.
Seo, Go Hun; Kim, Yoon-Myung; Oh, Seak Hee; Chung, Sun Ju; Choi, In Hee; Kim, Gu-Hwan; Yum, Mi-Sun; Choi, Jin-Ho; Kim, Kyung Mo; Ko, Tae-Sung; Lee, Beom Hee; Yoo, Han-Wook.
Afiliación
  • Seo GH; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim YM; Department of Pediatrics, Jeju National University School of Medicine, Jeju, Korea.
  • Oh SH; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Chung SJ; Department of Neurology, Asan Medical Center, Seoul, Korea.
  • Choi IH; Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim GH; Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Yum MS; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Choi JH; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Kim KM; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Ko TS; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Lee BH; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
  • Yoo HW; Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
J Med Genet ; 55(9): 587-593, 2018 09.
Article en En | MEDLINE | ID: mdl-29618506
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cobre / ATPasas Transportadoras de Cobre / Degeneración Hepatolenticular / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2018 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cobre / ATPasas Transportadoras de Cobre / Degeneración Hepatolenticular / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2018 Tipo del documento: Article