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A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.
Esquiaveto-Aun, Adriana Mangue; De Mello, Maricilda Palandi; Paulino, Maria Fernanda Vanti Macedo; Minicucci, Walter José; Guerra-Júnior, Gil; De Lemos-Marini, Sofia Helena Valente.
Afiliación
  • Esquiaveto-Aun AM; Department of Pediatrics, School of Medical Sciences (FCM), State University of Campinas (UNICAMP), Campinas, SP Brazil ; Center of Molecular Biology and Genetic Engineering (CBMEG), UNICAMP, Campinas, Brazil ; Center for Investigation in Pediatrics (CIPED), FCM, UNICAMP, Campinas, Brazil.
  • De Mello MP; Center of Molecular Biology and Genetic Engineering (CBMEG), UNICAMP, Campinas, Brazil.
  • Paulino MF; Department of Pediatrics, School of Medical Sciences (FCM), State University of Campinas (UNICAMP), Campinas, SP Brazil.
  • Minicucci WJ; Division of Endocrinology, Department of Clinical Medicine, FCM, UNICAMP, Campinas, Brazil.
  • Guerra-Júnior G; Department of Pediatrics, School of Medical Sciences (FCM), State University of Campinas (UNICAMP), Campinas, SP Brazil ; Center for Investigation in Pediatrics (CIPED), FCM, UNICAMP, Campinas, Brazil.
  • De Lemos-Marini SH; Department of Pediatrics, School of Medical Sciences (FCM), State University of Campinas (UNICAMP), Campinas, SP Brazil ; Center for Investigation in Pediatrics (CIPED), FCM, UNICAMP, Campinas, Brazil.
Diabetol Metab Syndr ; 7: 101, 2015.
Article en En | MEDLINE | ID: mdl-26587058
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Diabetol Metab Syndr Año: 2015 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Diabetol Metab Syndr Año: 2015 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Reino Unido