A Novel GNAS1 Mutation, R201G, in McCune–Albright Syndrome-Reference-Cited by-同舟云学术

A Novel GNAS1 Mutation, R201G, in McCune–Albright Syndrome

Published:1999-11-01 Issue:11 Volume:14 Page:1987-1989
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:

Author:

Riminucci Mara¹,Fisher Larry W.²,Majolagbe Adesola²,Corsi Alessandro¹,Lala Roberto³,De Sanctis Carlo³,Robey Pamela Gehron²,Bianco Paolo¹

Affiliation:

1. Dipartimento di Medicina Sperimentale, Universitá dell'Aquila, L'Aquila, Italy

2. Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, U.S.A.

3. Divisione di Endocrinologia Pediatrica, Ospedale Regina Margherita, Turin, Italy

Publisher

Oxford University Press (OUP)

Link

https://academic.oup.com/jbmr/article-pdf/14/11/1987/56598759/5650141122.pdf

Reference13 articles.

1. Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome;Schwindinger;Proc Natl Acad Sci USA,1992

2. An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome;Shenker;J Clin Endocrinol Metab,1994

3. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome;Weinstein;N Engl J Med,1991

4. Hydrolysis of GTP by the alpha-chain of Gs and other GTP binding proteins;Bourne;Proteins,1989

5. Inborn errors of signal transduction: Mutations in G proteins and G protein-coupled receptors as a cause of disease;Spiegel;J Inherit Metab Dis,1997

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