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Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report.
Papez, Jan; Starha, Jiri; Slaba, Katerina; Hubacek, Jaroslav A; Pecl, Jakub; Aulicka, Stefania; Urik, Milan; Ceylaner, Serdar; Vesela, Petra; Slaby, Ondrej; Jabandziev, Petr.
Afiliação
  • Papez J; Department of Pediatrics, University Hospital Brno, Brno, Czech Republic.
  • Starha J; Faculty of Medicine, Masaryk University, Brno, Czech Republic.
  • Slaba K; Department of Pediatrics, University Hospital Brno, Brno, Czech Republic.
  • Hubacek JA; Faculty of Medicine, Masaryk University, Brno, Czech Republic.
  • Pecl J; Department of Pediatrics, University Hospital Brno, Brno, Czech Republic.
  • Aulicka S; Faculty of Medicine, Masaryk University, Brno, Czech Republic.
  • Urik M; Experimental Medicine Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Ceylaner S; 3rd Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Vesela P; Department of Pediatrics, University Hospital Brno, Brno, Czech Republic.
  • Slaby O; Faculty of Medicine, Masaryk University, Brno, Czech Republic.
  • Jabandziev P; Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub ; 165(4): 454-457, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34012148
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Cátion TRPM / Hipocalcemia / Deficiência de Magnésio Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: República Tcheca
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Cátion TRPM / Hipocalcemia / Deficiência de Magnésio Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: República Tcheca