A case of mild phenotype Alport syndrome caused by COL4A3 mutations.

Kamijo, Masafumi; Kitamura, Mineaki; Muta, Kumiko; Uramatsu, Tadashi; Obata, Yoko; Nozu, Kandai; Kaito, Hiroshi; Iijima, Kazumoto; Mukae, Hiroshi; Nishino, Tomoya

Kamijo, Masafumi; Kitamura, Mineaki; Muta, Kumiko; Uramatsu, Tadashi; Obata, Yoko; Nozu, Kandai; Kaito, Hiroshi; Iijima, Kazumoto; Mukae, Hiroshi; Nishino, Tomoya.

Afiliação

Kamijo M; Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Kitamura M; Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan. minekitamura@nagasaki-u.ac.jp.
Muta K; Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Uramatsu T; Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Obata Y; Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kaito H; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Mukae H; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
Nishino T; Department of Nephrology, Nagasaki University Hospital, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.

CEN Case Rep ; 6(2): 189-193, 2017 Nov.

Article em En | MEDLINE | ID: mdl-28856578

Palavras-chave

Alport syndrome; The type IV collagen α3 chain (COLA4A3)

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: CEN Case Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão País de publicação: Japão

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google