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 (Journal Indexed in SCI) identifier

  • Publication Type: Article / Abstract
  • Volume: 86
  • Publication Date: 2016
  • Title of Journal : HORMONE RESEARCH IN PAEDIATRICS
  • Page Numbers: pp.431-432