Leydig Cell Hypoplasia due to Inactivating Luteinizing Hormone/Chorionic Gonadotropin Receptor Gene Mutation Presenting as a 46,XY DSD
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4419-8002-1_32.pdf
Reference3 articles.
1. Richter-Unruh A, Martens JW et al (2002) Leydig cell hypoplasia: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene. Clin Endocrinol (Oxf) 56:103–112.
2. McFarland KC, Sprengel R et al (1989) Lutropin-choriogonadotropin receptor: an unusual member of the G protein-coupled receptor family. Science 245:494–499.
3. Wu SM, Hallermeier KM et al (1998) Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasia. Mol Endocrinol 12:1651–1660.
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