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Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine Leiomyomas of Saudi Arabian Women
MED12, a subunit of mediator complex genes is known to harbor genetic mutations, (mostly in exon 2), causal to the genesis of uterine leiomyomas among Caucasian, African American, and Asian women. However, the precise relationship between genetic mutations vs. protein or disease phenotype is not wel...
Autores principales: | Ajabnoor, Ghada M. A., Mohammed, Nesma Amin, Banaganapalli, Babajan, Abdullah, Layla Saleh, Bondagji, Ola Nabeel, Mansouri, Nisma, Sahly, Nora Naif, Vaidyanathan, Venkatesh, Bondagji, Nabeel, Elango, Ramu, Shaik, Noor Ahmad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302612/ https://www.ncbi.nlm.nih.gov/pubmed/30619444 http://dx.doi.org/10.3389/fgene.2018.00552 |
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