Mutation analysis of the KAL gene in female patients with gonadotropin-releasing hormone deficiency

Isolated gonadotropin-releasing hormone (GnRH) deficiency, including Kallmann's syndrome (KS) and idiopathic hypogonadotropic hypogonadism (IHH), is a congenital disorder, which is characterized by a functional deficit in hypothalamic GnRH secretion. Despite recent advances in the understanding...

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Veröffentlicht in:	Yonsei medical journal 2004-02, Vol.45 (1), p.107-112
Hauptverfasser:	Lee, Sook-Hwan, Han, Jung-Hee, Cho, Sung-Won, Lee, Whee-Hyun, Cha, Kwang-Yul, Lee, Mee-Hwa
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult DNA Mutational Analysis Extracellular Matrix Proteins - genetics Female Gonadotropin-Releasing Hormone - deficiency Humans Kallmann Syndrome - genetics Kallmann Syndrome - metabolism Nerve Tissue Proteins - genetics Phenotype Polymorphism, Single-Stranded Conformational
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