Mutation Spectra in Fragile X Syndrome Induced by Deletions of CGG·CCG Repeats
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference50 articles.
1. Genetic Instabilities and Neurological Diseases,2006
2. Trinucleotide Repeat Disorders
3. DNA structures, repeat expansions and human hereditary disorders
4. Non-B DNA structure-induced genetic instability
5. Chromatin structure of repeating CTG/CAG and CGG/CCG sequences in human disease
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4. Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes;Genes;2021-10-22
5. Spontaneous rescue of a FMR1 repeat expansion and review of deletions in the FMR1 non-coding region;European Journal of Medical Genetics;2021-08
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