A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients

BACKGROUND: The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is present in at least 1 out of 4,500 female live births and is the second most common cause for primary amenorrhea. It is characterized by vaginal and uterine aplasia in an XX individual with normal secondary characteristics. It has lon...

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Detalles Bibliográficos
Autores principales: Rall, Katharina, Barresi, Gianmaria, Walter, Michael, Poths, Sven, Haebig, Karina, Schaeferhoff, Karin, Schoenfisch, Birgitt, Riess, Olaf, Wallwiener, Diethelm, Bonin, Michael, Brucker, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123171/
https://www.ncbi.nlm.nih.gov/pubmed/21619687
http://dx.doi.org/10.1186/1750-1172-6-32

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