Klaus Mohnike
0000-0001-5113-8657
3 papers found
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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
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome [version 2; peer review: 3 approved]
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