A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 11756613.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Autosomal dominant progressive external ophthalmoplegia (adPEO) is caused by mutations in at least three different genes: ANT1 (chromosome 4q34-35), TWINKLE, and POLG. The ANT1 gene encodes the adenine nucleotide translocator-1 (ANT1). We identified a heterozygous T293C mutation of the ANT1 gene in a Greek family with adPEO. The resulting leucine to proline substitution likely modifies the secondary structure of the ANT1 protein. ANT1 gene mutations may account for adPEO in families with different ethnic backgrounds.
Medical subject headings
- Adenine Nucleotide Translocator 1
- Chromosomes, Human, Pair 4
- Mutation, Missense
- Ophthalmoplegia, Chronic Progressive External