Certain Activating Mutations within Helix 6 of the Human Luteinizing Hormone Receptor May Be Explained by Alterations That Allow Transmembrane Regions to Activate Gs
Author:
Affiliation:
1. Department of Physiology and Biophysics (A.N.A., D.L.S.) The University of Iowa College of Medicine Iowa City, Iowa 52242
2. Department of Biochemistry and Molecular Biology (D.J.M.) Mayo Clinic/Mayo Foundation Rochester, Minnesota 55905
Publisher
The Endocrine Society
Subject
Endocrinology,Molecular Biology,General Medicine
Link
http://academic.oup.com/mend/article-pdf/12/12/1857/8953824/mend1857.pdf
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3. A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty.;Shenker;Nature,1993
4. Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.;Laue;Proc Natl Acad Sci USA,1995
5. A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty.;Latronico;J Clin Endocrinol Metab,1995
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