Your browser doesn't support javascript.
loading
Defective C3d caused by C3 p.W1034R in inherited atypical hemolytic uremic syndrome.
Tsuchida, Masafumi; Goto, Shin; Watanabe, Hirofumi; Goto, Sawako; Yamaguchi, Hiroki; Narita, Ichiei.
Afiliação
  • Tsuchida M; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Goto S; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Watanabe H; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Goto S; Department of Applied Molecular Medicine, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Yamaguchi H; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Narita I; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Mol Genet Genomic Med ; 12(1): e2288, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37795781
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome Hemolítico-Urêmica Atípica Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome Hemolítico-Urêmica Atípica Idioma: En Ano de publicação: 2024 Tipo de documento: Article