Associated Papers
Novel p.Arg534del Mutation and MTHFR C667T Polymorphism in Fragile X Syndrome (FXS) With Autism Spectrum Phenotype: A Case Report.
Hasan H et al.
Case Reports in Genetics, 2025
In Silico Analysis of FMR1 Gene Missense SNPs.
Tekcan A
Cell Biochemistry and Biophysics, 2016
Epimutations in human disease.
Horsthemke B
Current Topics in Microbiology and Immunology, 2006
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