Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I
Author:
Funder
National Research Centre
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s42000-020-00226-6.pdf
Reference38 articles.
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2. Latronico AC, Arnhold IJ (2012) Inactivating mutations of the human luteinizing hormone receptor in both sexes. Semin Reprod Med 30(5): 382–386.
3. Ulloa-Aguirre A, Stanislaus D, Arora V, Väänänen J, Brothers S, Janovick JA et al (1998) The third intracellular loop of the rat gonadotropin-releasing hormone receptor couples the receptor to Gs-and Gq/11-mediated signal transduction pathways: evidence from loop fragment transfection in GGH3 cells. Endocrinology. 139(5):2472–2478
4. Gershengorn MC, Osman R (2001) Minireview: insights into G protein-coupled receptor function using molecular models. Endocrinology. 142(1):2–10
5. Haider SG (2004) Cell biology of Leydig cells in the testis. Int Rev Cytol 233(4):181–241
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