Pathogenic variants of Alport syndrome and monogenic diabetes identified by exome sequencing in a family.

Watanabe, Hirofumi; Goto, Shin; Hosojima, Michihiro; Kabasawa, Hideyuki; Imai, Naofumi; Ito, Yumi; Narita, Ichiei

Watanabe, Hirofumi; Goto, Shin; Hosojima, Michihiro; Kabasawa, Hideyuki; Imai, Naofumi; Ito, Yumi; Narita, Ichiei.

Afiliação

Watanabe H; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan. watanabeh@med.niigata-u.ac.jp.
Goto S; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Hosojima M; Department of Clinical Nutrition Science, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Kabasawa H; Department of Clinical Nutrition Science, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Imai N; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Ito Y; Division of Clinical Nephrology and Rheumatology, Kidney Research Center, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Narita I; Department of Health Promotion Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Hum Genome Var ; 10(1): 5, 2023 Feb 02.

Article em En | MEDLINE | ID: mdl-36732323

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Hum Genome Var Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

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