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
Chemical and structural probing of the N-terminal residues encoded by FMR1 exon 15 and their effect on downstream arginine methylation.
Dolzhanskaya N et al.
Biochemistry, 2008
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