Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene

Ozturk M. N., Demirbilek H., KOTAN L. D., Baysal B., Ocal M., TOPALOĞLU A. K.

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.431-432, 2016 (SCI-Expanded, Scopus)

  • Publication Type: Article / Abstract
  • Volume: 86
  • Publication Date: 2016
  • Journal Name: HORMONE RESEARCH IN PAEDIATRICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.431-432
  • Hacettepe University Affiliated: Yes