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Functional study of an aberrant splicing variant of the human luteinizing hormone (LH) receptor
The luteinizing hormone receptor (LHR) is a member of a subfamily of G protein-coupled receptors that is characterized by its alternative splicing. In a previous study, we identified a splice site mutation of intron 6 (IVS6-3C>A) in a patient suffering from Leydig cell hypoplasia, which leads to...
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| Autori principali: | , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3292396/ https://ncbi.nlm.nih.gov/pubmed/22002533 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/molehr/gar065 |
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