Article
The fragile X syndromes.
Seminars in cell biology - 1 Feb 1995
Nelson D L
Abstract excerpt
Fragile X syndrome is a leading cause of mental retardation worldwide, with an incidence of approximately one case in 2000 live births. It is amongst the most common of human genetic diseases, and was the first to be associated with an unstable trinucleotide (CGG) repeat sequence. It is also char...
Topics
- Animals
- Chromosome Fragile Sites
- Chromosome Fragility
- Fragile X Mental Retardation Protein
- Fragile X Syndrome
- Humans
- Mutation
- Nerve Tissue Proteins
- RNA-Binding Proteins
- Repetitive Sequences, Nucleic Acid
