Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes.

Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes. Genes (Basel). 2021 10 22; 12(11).

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subject areas

5' Untranslated Regions
Adult
Female
Fragile X Mental Retardation Protein
Fragile X Syndrome
Gene Frequency
Genetic Association Studies
Humans
Infant
Infant, Newborn
Male
Mutation
Open Reading Frames
Pregnancy
RNA, Messenger
Sequence Deletion
Trinucleotide Repeat Expansion
Trinucleotide Repeats

authors with profiles

Sho Yano