Low-normal FMR1 CGG repeat length: phenotypic associations

This population-based study investigates genotype–phenotype correlations of “low- normal” CGG repeats in the fragile X mental retardation 1 (FMR1) gene. FMR1 plays an important role in brain development and function, and encodes FMRP (fragile X mental retardation protein), an RNA-binding protein tha...

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Detalhes bibliográficos
Main Authors: Mailick, Marsha R., Hong, Jinkuk, Rathouz, Paul, Baker, Mei W., Greenberg, Jan S., Smith, Leann, Maenner, Matthew
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2014
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4158814/
https://ncbi.nlm.nih.gov/pubmed/25250047
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00309
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