A G‐protein Subunit‐α11 Loss‐of‐Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)-Reference-Cited by-同舟云学术

A G‐protein Subunit‐α11 Loss‐of‐Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)

Author:

Gorvin Caroline M¹,Cranston Treena²,Hannan Fadil M¹³,Rust Nigel⁴,Qureshi Asjid⁵,Nesbit M Andrew¹⁶,Thakker Rajesh V¹

Affiliation:

1. Academic Endocrine Unit, Radcliffe Department of MedicineUniversity of OxfordOxfordUK

2. Oxford Molecular Genetics Laboratory, Churchill HospitalOxfordUK

3. Department of Musculoskeletal Biology, Institute of Ageing and Chronic DiseaseUniversity of LiverpoolLiverpoolUK

4. Sir William Dunn School of PathologyUniversity of OxfordOxfordUK

5. Department of Diabetes and EndocrinologyNorthwest London NHS TrustLondonUK

6. School of Biomedical SciencesUniversity of UlsterColeraineLondonderryUK

Funder

Medical Research Council

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

Reference36 articles.

4. Activation of phospholipase C by the alpha subunits of the Gq and G11 proteins in transfected Cos‐7 cells;Wu DQ;J Biol Chem,1992

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