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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Autori principali: Rall, Katharina, Barresi, Gianmaria, Walter, Michael, Poths, Sven, Haebig, Karina, Schaeferhoff, Karin, Schoenfisch, Birgitt, Riess, Olaf, Wallwiener, Diethelm, Bonin, Michael, Brucker, Sara
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2011
Soggetti:
Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3123171/
https://ncbi.nlm.nih.gov/pubmed/21619687
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-32
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