What is the genetic malformation associated near Friedrich's ataxia?
Answer:
Friedreich ataxia is inherited as an autosomal recessive disorder. It is due to an abnormality surrounded by a gene called, frataxin mitochondrial protein, which is located on chromosome 9. .
The genetic malformation associated with Friedrich's ataxia is an autosomal and recessive mutation. It is a mutation surrounded by gene X25 which encodes frataxin, a protein whose function is not entirely clear but which does localize to the mitochondria. The gene encoding frataxin is found on human chromosome 9. The genetic defect associated beside Friedrich's ataxia is found within the intronic sequence which probable results in silencing (and as a consequence non-expression) of this gene.