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A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature.
Li, Shentang; Yang, Yeyi; Huang, Lihua; Kong, Min; Yang, Zuocheng.
Afiliação
  • Li S; Department of Pediatrics, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
  • Yang Y; Department of Medicine, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
  • Huang L; Central Laboratory, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
  • Kong M; Department of Pediatrics, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
  • Yang Z; Department of Pediatrics, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P.R. China.
Mol Med Rep ; 19(5): 4364-4376, 2019 May.
Article em En | MEDLINE | ID: mdl-30942416
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Povo Asiático / Transportador 2 de Glucose-Sódio / Glicosúria Renal Tipo de estudo: Prognostic_studies Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Povo Asiático / Transportador 2 de Glucose-Sódio / Glicosúria Renal Tipo de estudo: Prognostic_studies Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article