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A novel heterozygous mutation of CHD7 gene in a Chinese patient with Kallmann syndrome: a case report
Variants of chromodomain helicase DNA binding protein 7 (CHD7) gene are commonly associated with Kallmann syndrome (KS) and account for 5–6% of idiopathic hypogonadotropic hypogonadism (IHH) cases. Here we rep...
Citation: BMC Endocrine Disorders 2021 21:193