Different Biochemical Properties Explain Why Two Equivalent Gα Subunit Mutants Cause Unrelated Diseases

There is an increasing number of disease-associated Gα mutations identified from genome-wide sequencing campaigns or targeted efforts. Albright's Hereditary Osteodystrophy (AHO) was the first inherited disease associated with loss-of-function mutations in a G protein (Gαs) and other studies rev...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Leyme, Anthony, Marivin, Arthur, Casler, Jason, Nguyen, Lien T., Garcia-Marcos, Mikel
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Biochemistry and Molecular Biology 2014
Gaiak:
Molecular Bases of Disease
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4139202/
https://ncbi.nlm.nih.gov/pubmed/24982418
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M114.549790
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