Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.

No abstract is available for this paper.

• Publication year

  2014

• Venue

  European Journal of Endocrinology

• Publication date

  2014-06-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1530/EJE-14-0045PMID 24686051
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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