A heterozygous 4-bp deletion mutation in the Gsα gene (GNAS1) in a patient with albright hereditary osteodystrophy
- 31 August 1992
- Vol. 13 (4) , 1319-1321
- https://doi.org/10.1016/0888-7543(92)90056-x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- The role of G-protein in matrix-mediated motility of highly and poorly invasive melanoma cellsInternational Journal of Cancer, 2007
- Activating Mutations of the Stimulatory G Protein in the McCune–Albright SyndromeNew England Journal of Medicine, 1991
- Genetic mapping of the Gs-α subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresisGenomics, 1991
- Translation to near the distal end of the penultimate exon is required for normal levels of spliced triosephosphate isomerase mRNA.Molecular and Cellular Biology, 1990
- Two G Protein Oncogenes in Human Endocrine TumorsScience, 1990
- Mutation in the Gene Encoding the Stimulatory G Protein of Adenylate Cyclase in Albright's Hereditary OsteodystrophyNew England Journal of Medicine, 1990
- A gel electrophoretic assay for detecting the insertion defect in Ashkenazi Jewish carriers of Tay-Sachs diseaseAnalytical Biochemistry, 1990
- Nonsense mutations in the dihydrofolate reductase gene affect RNA processing.Molecular and Cellular Biology, 1989
- Activity of the Stimulatory Guanine Nucleotide-Binding Protein Is Reduced in Erythrocytes from Patients with Pseudohypoparathyroidism and Pseudopseudohypoparathyroidism: Biochemical, Endocrine, and Genetic Analysis of Albright's Hereditary Osteodystrophy in Six Kindreds*Journal of Clinical Endocrinology & Metabolism, 1986