Spectral Analysis of Codons in the DNA Sequence of Fragile X Syndrome.
There are frequent studies undergoing related to the Fragile X syndrome caused due to the triplet CGG replicates on the X chromosome of Fragile X Mental Retardation 1 (FMR1) gene. Mutations of this chromosome can lead to Fragile X syndrome, rational disability, and other cognitive discrepancies. A n...
| Publicado en: | Journal of Medical Systems Vol. 43; no. 8 |
|---|---|
| Autores principales: | , |
| Formato: | equations & formulas tables/charts Journal Article |
| Publicado: |
Springer Nature
Aug2019
|
| Acceso en línea: | Ver este registro en EBSCOhost |