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X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansion

The Fragile X-related disorders are X-linked disorders resulting from the inheritance of FMR1 alleles with >54 CGG/CCG repeats in their 5′ UTR. The repeats expand both somatically and on intergenerational transmission and increased repeat numbers are associated with increased risk of disease and...

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Detalhes bibliográficos
Main Authors: Adihe Lokanga, Rachel, Zhao, Xiao-Nan, Entezam, Ali, Usdin, Karen
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4140472/
https://ncbi.nlm.nih.gov/pubmed/24858908
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu213
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