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Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene.
Acar, Filiz Aktürk; Isik, Günes; Mutlu, Mehmet; Kader, Sebnem; Aslan, Yakup; Kalyoncu, Mukaddes.
Afiliação
  • Acar FA; Division of Neonatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
  • Isik G; Department of Pediatric Nephrology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
  • Mutlu M; Division of Neonatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
  • Kader S; Division of Neonatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
  • Aslan Y; Division of Neonatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
  • Kalyoncu M; Department of Pediatric Nephrology and Rheumatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Indian J Nephrol ; 29(5): 360-363, 2019.
Article em En | MEDLINE | ID: mdl-31571745
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Indian J Nephrol Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Indian J Nephrol Ano de publicação: 2019 Tipo de documento: Article