KAL |
KALI |
S1 protein |
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[Kallmann syndrome 2] This entity is characterized primarily by hypogonadotropic hypogonadism and anosmia. One of the causes are loss-of-function mutations in the receptor for the two fibroblast growth factors, aFGF and bFGF (Dode et al, 2003). See: FGFR1.
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