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Long-Read Sequencing Identifies Mosaic Sequence Variations in Friedreich's Ataxia-GAA Repeats
Joohyun Park1, Claudia Dufke1, Zofia Fleszar2
1Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany.
This study details a complex Friedreich's ataxia (FRDA) case diagnosed using advanced genome sequencing. Long-read sequencing revealed intricate GAA repeat expansions and mosaic variations, improving diagnostic accuracy for this neurodegenerative disorder.
Area of Science:
- Genetics
- Neurodegenerative Disorders
- Genomic Medicine
Background:
- Friedreich's ataxia (FRDA) is an autosomal recessive neurodegenerative disorder.
- Most FRDA cases result from GAA trinucleotide repeat expansions in the FXN gene.
- A subset of patients have compound heterozygous genotypes involving a GAA repeat expansion and a pathogenic small variant.
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