Associated Papers
Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations.
Nie M et al.
European Journal of Endocrinology, 2017
Point mutations in KAL1 and the mitochondrial gene MT-tRNA(cys) synergize to produce Kallmann syndrome phenotype.
Wang F et al.
Scientific Reports, 2015
The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome.
Zhang S et al.
Fertility and Sterility, 2013
X-linked GnRH deficiency: role of KAL-1 mutations in GnRH deficiency.
Hu Y et al.
Molecular and Cellular Endocrinology, 2011
Identification of two novel missense mutations in the KAL1 gene in Han Chinese subjects with Kallmann Syndrome.
Jap TS et al.
Journal of Endocrinological Investigation, 2011
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