M.A. D. Gigonzac
Publications of : M.A. D. Gigonzac
Human Genetics Research Article
Molecular Diagnosis of X-Fragile Syndrome: Perspectives for the Public Health System in the Central Region of Brazil
X-Fragile Syndrome (FXS) is the most common cause of inherited intellectual disability and the second of genetic origin, with an estimated prevalence of 1/4000 men and 1/6000 women. The etiology is associated with a trinucleotide expansion of CGG sequences and hypermethylation of the promoter region of the FMR1 (Fragile-X Mental Retardation-1) gene, located in the X.. Read More»
Genet. Mol. Res. 16(4): gmr16039848
DOI: 10.4238/gmr16039848
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Citations : 56184
Genetics and Molecular Research received 56184 citations as per google scholar report
