A novel heterozygous intron mutation in SEMA7A causing kallmann syndrome in a female
Author:
Affiliation:
1. Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, PR China;
2. Translational Medicine Research and Cooperation Center of Northern China, Heilongjiang Academy of Medical Sciences, Harbin, China
Publisher
Informa UK Limited
Subject
Obstetrics and Gynaecology,Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.tandfonline.com/doi/pdf/10.1080/09513590.2019.1680624
Reference19 articles.
1. Kallmann syndrome
2. The Complex Genetics of Kallmann Syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.
3. Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future
4. Gonadotropin-releasing hormone (GnRH) neuron migration: Initiation, maintenance and cessation as critical steps to ensure normal reproductive function
5. GnRH, anosmia and hypogonadotropic hypogonadism – Where are we?
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