Klaus Mohnike
0000-0001-5113-8657
3 papers found
Refreshing results…
Pasireotide treatment for severe congenital hyperinsulinism due to a homozygous ABCC8 mutation
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome [version 2; peer review: 3 approved]
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
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