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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158814/ https://www.ncbi.nlm.nih.gov/pubmed/25250047 http://dx.doi.org/10.3389/fgene.2014.00309 |