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Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.
A model is developed to account for recent molecular observations. It postulates four alleles: normal (N), small rather stable insert (S), larger, unstable insert (Z), and large insert (L). The last-named allele causes the fragile-X phenotype, inactivation of the FMR1 locus by methylation, and menta...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1992
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC525664/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1570349/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.9.4215 |
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