TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

BACKGROUND: Müllerian aplasia (MA) is a congenital disorder of the female reproductive tract with absence of uterus and vagina with paramount impact on a woman’s life. Despite intense research, no major genes have been found to explain the complex genetic etiology. METHODS AND RESULTS: We have used...

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Detalhes bibliográficos
Main Authors: Sandbacka, Maria, Laivuori, Hannele, Freitas, Érika, Halttunen, Mervi, Jokimaa, Varpu, Morin-Papunen, Laure, Rosenberg, Carla, Aittomäki, Kristiina
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3847609/
https://ncbi.nlm.nih.gov/pubmed/23954021
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-125
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