GCM2 -Activating Mutations in Familial Isolated Hyperparathyroidism-Reference-Cited by-同舟云学术

GCM2 -Activating Mutations in Familial Isolated Hyperparathyroidism

Published:2016-11 Issue:5 Volume:99 Page:1034-1044
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guan Bin,Welch James M.,Sapp Julie C.,Ling Hua,Li Yulong,Johnston Jennifer J.,Kebebew Electron,Biesecker Leslie G.,Simonds William F.,Marx Stephen J.,Agarwal Sunita K.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference42 articles.

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2. The diagnosis and management of asymptomatic primary hyperparathyroidism;Silverberg;Nat. Clin. Pract. Endocrinol. Metab.,2006

3. Genetic defects associated with familial and sporadic hyperparathyroidism;Hendy;Front. Horm. Res.,2013

4. Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene;Hannan;Nat. Clin. Pract. Endocrinol. Metab.,2008

5. Medical management of primary hyperparathyroidism: proceedings of the fourth International Workshop on the Management of Asymptomatic Primary Hyperparathyroidism;Marcocci;J. Clin. Endocrinol. Metab.,2014

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