A needle in a haystack: Mutations in GNRH1 as a rare cause of isolated GnRH deficiency
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Molecular Biology,Biochemistry
Reference47 articles.
1. Purification, amino acid composition and N-terminus of the hypothalamic luteinizing hormone releasing factor (LRF) of ovine origin;Amoss;Biochem. Biophys. Res. Commun.,1971
2. Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes;Bo-Abbas;J. Clin. Endocrinol. Metab.,2003
3. Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation;Bouligand;N. Engl. J. Med.,2009
4. Genetics defects in GNRH1: a paradigm of hypothalamic congenital gonadotropin deficiency;Bouligand;Brain Res.,2010
5. A genetic basis for functional hypothalamic amenorrhea;Caronia;N. Engl. J. Med.,2011
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1. Idiopathic hypogonadotropic hypogonadism caused by compound heterozygosity for two novel mutations in the GNRH1 gene: a case report;BMC Endocrine Disorders;2023-10-05
2. Review of human genetic and clinical studies directly relevant to GnRH signalling;Journal of Neuroendocrinology;2021-12-31
3. GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review;Neuroendocrinology;2021-12-17
4. The cryptic gonadotropin-releasing hormone neuronal system of human basal ganglia;eLife;2021-06-15
5. The cryptic gonadotropin-releasing hormone neuronal system of human basal ganglia;2021-03-06
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