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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
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

Internet

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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