Title : The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.

Pub. Date : 1998 Aug

PMID : 10732799






4 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Most cases of Friedreich ataxia (FRDA) are due to expansions of a GAA trinucleotide repeat sequence in the FRDA gene coding for frataxin, a protein of poorly understood function which may regulate mitochondrial iron transport. Iron frataxin Homo sapiens
2 Most cases of Friedreich ataxia (FRDA) are due to expansions of a GAA trinucleotide repeat sequence in the FRDA gene coding for frataxin, a protein of poorly understood function which may regulate mitochondrial iron transport. Iron frataxin Homo sapiens
3 Most cases of Friedreich ataxia (FRDA) are due to expansions of a GAA trinucleotide repeat sequence in the FRDA gene coding for frataxin, a protein of poorly understood function which may regulate mitochondrial iron transport. Iron frataxin Homo sapiens
4 Most cases of Friedreich ataxia (FRDA) are due to expansions of a GAA trinucleotide repeat sequence in the FRDA gene coding for frataxin, a protein of poorly understood function which may regulate mitochondrial iron transport. Iron frataxin Homo sapiens