https://www.selleckchem.com/pr....oducts/PD-0325901.ht
Kallmann syndrome (KS) is a genetically heterogeneous condition characterized by hypogonadotropic hypogonadism (HH) and olfactory dysfunction. Although , a causative gene for Waardenburg syndrome (WS) and peripheral demyelinating neuropathy, central demyelination, WS, and Hirschsprung disease (PCWH) has previously been implicated in KS, the clinical significance of variants as the cause of KS remains uncertain. A total of 117 patients with KS underwent mutation screening of and 14 other causative genes for KS/HH. Rare variants were s
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