Hyperinsulinism in a patient with a Zellweger Spectrum Disorder and a 16p11.2 deletion syndrome
Mol Genet Metab Rep
.
2020 Apr 28:23:100590.
doi: 10.1016/j.ymgmr.2020.100590.
eCollection 2020 Jun.
Authors
Eva M M Hoytema van Konijnenburg
1
,
Ilse K Luirink
1
,
Sebastian E E Schagen
2
,
Marc Engelen
3
,
Kevin Berendse
1
,
Bwee Tien Poll-The
2
3
,
Malika Chegary
2
Affiliations
1
Department of Pediatrics, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
2
Department of Pediatrics, OLVG Hospital, Jan Tooropstraat 164 1061 AE, Amsterdam, the Netherlands.
3
Department of Pediatric Neurology, Emma Children's Hospital, Amsterdam UMC, Meibergdreef 9 1105, AZ, Amsterdam, the Netherlands.
PMID:
32373468
PMCID:
PMC7191845
DOI:
10.1016/j.ymgmr.2020.100590
No abstract available