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Paper Details

Ethnicity of Patients With Germline <i>GCM2</i>-Activating Variants and Primary Hyperparathyroidism.
J Endocr Soc
21
2017
C, CCID, Diabetes, Digestive and Kidney Diseases, FIHP, GCM2, GCM2 CCID region, GCM2 variants, GCM2-, GCM2-Activating Variants, Leu379Gln, Luciferase, Luciferase reporter, PHPT, Patients, Primary Hyperparathyroidism, Tyr394Ser, a, amino acid, blood, blood DNA, c.1136T, c.1181A, familial isolated hyperparathyroidism, p, p., patient, patients, primary hyperparathyroidism, sporadic PHPT, transcription factor GCM2
Author NameAffiliation
Hua LingThe Center for Inherited Disease Research, Johns Hopkins University
Electron KebebewThe National Cancer Institute
Electron KebebewThe National Cancer Institute
William F SimondsThe National Institute of Diabetes and Digestive and Kidney Diseases
Stephen J MarxThe National Institute of Diabetes and Digestive and Kidney Diseases
Stephen J MarxThe Eunice Kennedy Shriver National Institute of Child Health and Human Development
Stephen J MarxThe National Institute of Diabetes and Digestive and Kidney Diseases
Stephen J MarxThe Eunice Kennedy Shriver National Institute of Child Health and Human Development
Sunita K AgarwalThe National Institute of Diabetes and Digestive and Kidney Diseases
Sunita K AgarwalThe National Institute of Diabetes and Digestive and Kidney Diseases
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