Clinical characteristics and phenotype–genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations
Year: 2014
Type: article
Study design: Observational Study
DOI: 10.1530/eje-14-0045
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: closed
Funder: University College London
OpenAlex ID: W2096951558
