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SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS.
Karakilic-Ozturan, E; Ozturk, A P; Oney, C; Kardelen Al, A D; Yildirim, Z Y; Balci, H I; Poyrazoglu, S; Bas, F; Darendeliler, F.
Afiliación
  • Karakilic-Ozturan E; Dept. of Pediatric Endocrinology and Diabetes, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Ozturk AP; Dept. of Pediatric Endocrinology and Diabetes, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Oney C; Dept. of Pediatrics, Istanbul University, Istanbul Faculty of Medicine Istanbul, Turkey.
  • Kardelen Al AD; Dept. of Pediatric Endocrinology and Diabetes, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Yildirim ZY; Dept. of Pediatric Nephrology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Balci HI; Dept. of Orthopedics and Traumatology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Poyrazoglu S; Dept. of Pediatric Endocrinology and Diabetes, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Bas F; Dept. of Pediatric Endocrinology and Diabetes, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Darendeliler F; Dept. of Pediatric Endocrinology and Diabetes, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
Acta Endocrinol (Buchar) ; 18(3): 387-391, 2022.
Article en En | MEDLINE | ID: mdl-36699160
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Acta Endocrinol (Buchar) Año: 2022 Tipo del documento: Article País de afiliación: Turquía
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Acta Endocrinol (Buchar) Año: 2022 Tipo del documento: Article País de afiliación: Turquía