Jenniffer Villareal
Biographic Data
| ID | 7967095 |
|---|---|
| NAME | Jenniffer Villareal |
| GIVEN NAMES | Jenniffer |
| FAMILY NAME | Villareal |
| SIGNATURE | VILLAREAL J |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 1 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2021 |
| LATEST PUBLICATION YEAR | 2021 |
| H-INDEX | 0 |
Experiences of the Molecular Diagnosis of Fragile X Syndrome in Ecuador
Fragile X syndrome (FXS) is the most common cause of hereditary intellectual disability and the second most common cause of intellectual disability of genetic etiology. This complex neurodevelopmental disorder is caused by an alteration in the CGG trinucleotide expansion in fragile X mental retardation gene 1 ( FMR1 ) leading to gene silencing and the subsequent loss of its product: fragile X mental retardation protein 1 (FMRP). Molecular diagnos…
No prominent works on this page.
Experiences of the Molecular Diagnosis of Fragile X Syndrome in Ecuador
Fragile X syndrome (FXS) is the most common cause of hereditary intellectual disability and the second most common cause of intellectual disability of genetic etiology. This complex neurodevelopmental disorder is caused by an alteration in the CGG trinucleotide expansion in fragile X mental retardation gene 1 ( FMR1 ) leading to gene silencing and the subsequent loss of its product: fragile X mental retardation protein 1 (FMRP). Molecular diagnos…
Allele (1 works) · Autism Spectrum Disorder Research (1 works) · Biology (1 works) · Congenital heart defects research (1 works) · Disease (1 works) · FMR1 (1 works) · Fragile x (1 works) · Fragile X syndrome (1 works) · Gene (1 works) · Gene silencing (1 works)