Friedreich ataxia is an autosomal recessive disorder caused by mutations in the FRDA gene that encodes a 210-amino acid protein called frataxin. An expansion of a GAA trinucleotide repeat in intron 1 of the gene is present in more than 95% of mutant alleles. Of the 83 people we studied who have muta
Genetic variation in Australian isolates of myxoma virus: an evolutionary and epidemiological study
โ Scribed by K. M. Saint; N. French; P. Kerr
- Publisher
- Springer Vienna
- Year
- 2001
- Tongue
- English
- Weight
- 349 KB
- Volume
- 146
- Category
- Article
- ISSN
- 1432-8798
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