DNA Methylation Analysis of Turner Syndrome BAV

Turner Syndrome (TS) is a rare cytogenetic disorder caused by the complete loss or structural variation of the second sex chromosome. The most common cause of early mortality in TS results from a high incidence of left-sided congenital heart defects, including bicuspid aortic valve (BAV), which occu...

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Detalles Bibliográficos
Autores principales: Gutierrez, Jacob, Davis, Brett A., Nevonen, Kimberly A., Ward, Samantha, Carbone, Lucia, Maslen, Cheryl L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194862/
https://www.ncbi.nlm.nih.gov/pubmed/35711915
http://dx.doi.org/10.3389/fgene.2022.872750

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194862/
https://www.ncbi.nlm.nih.gov/pubmed/35711915
http://dx.doi.org/10.3389/fgene.2022.872750

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