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Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.

Affected members of most kindreds with Albright hereditary osteodystrophy have a partial deficiency of functional Gs, the guanine nucleotide-binding protein that stimulates adenylyl cyclase. By use of the polymerase chain reaction to amplify genomic fragments with the attachment of a high-melting G...

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Dettagli Bibliografici
Pubblicato in:Proc Natl Acad Sci U S A
Autori principali: Weinstein, L S, Gejman, P V, Friedman, E, Kadowaki, T, Collins, R M, Gershon, E S, Spiegel, A M
Natura: Artigo
Lingua:Inglês
Pubblicazione: National Academy of Sciences 1990
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Accesso online:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54940/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2122458/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.21.8287
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