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Hyperinsulinism in a patient with a Zellweger Spectrum Disorder and a 16p11.2 deletion syndrome.
Hoytema van Konijnenburg, Eva M M; Luirink, Ilse K; Schagen, Sebastian E E; Engelen, Marc; Berendse, Kevin; Poll-The, Bwee Tien; Chegary, Malika.
Afiliação
  • Hoytema van Konijnenburg EMM; Department of Pediatrics, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
  • Luirink IK; Department of Pediatrics, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
  • Schagen SEE; Department of Pediatrics, OLVG Hospital, Jan Tooropstraat 164 1061 AE, Amsterdam, the Netherlands.
  • Engelen M; Department of Pediatric Neurology, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
  • Berendse K; Department of Pediatrics, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
  • Poll-The BT; Department of Pediatrics, OLVG Hospital, Jan Tooropstraat 164 1061 AE, Amsterdam, the Netherlands.
  • Chegary M; Department of Pediatric Neurology, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
Mol Genet Metab Rep ; 23: 100590, 2020 Jun.
Article em En | MEDLINE | ID: mdl-32373468
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 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 Ano de publicação: 2020 Tipo de documento: Article