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Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor

Publikace na 1. lékařská fakulta, Lékařská fakulta v Plzni |
2009

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

A patient with partial hypogonadotropic hypogonadism caused by a compound heterozygous GnRH-R mutation was described. Two different mutations were identified by TGGE and direct sequencing: one in exon 1 (Gln106Arg) and the other in exon 3 (Leu266Arg).