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Novel dysfunctional variant in ABCG2 as a cause of severe tophaceous gout: biochemical, molecular genetics and functional analysis.
Stiburkova, Blanka; Miyata, Hiroshi; Závada, Jakub; Tomcík, Michal; Pavelka, Karel; Storkanova, Gabriela; Toyoda, Yu; Takada, Tappei; Suzuki, Hiroshi.
Afiliação
  • Stiburkova B; Institute of Rheumatology, Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic and stiburkova@revma.cz.
  • Miyata H; Department of Pharmacy, University of Tokyo Hospital, Tokyo, Japan.
  • Závada J; Institute of Rheumatology.
  • Tomcík M; Institute of Rheumatology.
  • Pavelka K; Institute of Rheumatology.
  • Storkanova G; Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic and.
  • Toyoda Y; Department of Pharmacy, University of Tokyo Hospital, Tokyo, Japan.
  • Takada T; Department of Pharmacy, University of Tokyo Hospital, Tokyo, Japan.
  • Suzuki H; Department of Pharmacy, University of Tokyo Hospital, Tokyo, Japan.
Rheumatology (Oxford) ; 55(1): 191-4, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26428519
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Transportadores de Cassetes de Ligação de ATP / Gota / Atividade Motora / Proteínas de Neoplasias Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Transportadores de Cassetes de Ligação de ATP / Gota / Atividade Motora / Proteínas de Neoplasias Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article