Friedreich ataxia (FRDA) is the commonest hereditary ataxia in Caucasians. Most patients are homozygous for expanded GAA triplet repeats in the first intron of the frataxin (FXN) gene, involved in mitochondrial iron metabolism. Here, we used magnetoencephalography (MEG) to characterize the main determinants of FRDA-related changes in intrinsic functional brain architecture.info:eu-repo/semantics/publishe
<div><p>Friedreich’s ataxia (FRDA) is a genetic neurodegenerative disorder caused by transcriptional...
AbstractFriedreich ataxia (FRDA) patients are homozygous for expanded GAA triplet-repeat alleles in ...
Friedreich’s ataxia (FRDA) is a rare genetic disorder caused by mutations in the gene frataxin, enco...
This magnetoencephalography (MEG) study addresses (i) how Friedreich ataxia (FRDA) affects the sub-s...
This magnetoencephalography (MEG) study addresses (i) how Friedreich ataxia (FRDA) affects the sub-s...
© 2011 Dr. Hamed AkhlaghiFriedreich ataxia (FRDA) is caused by mutations in the FXN gene leading to ...
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder that affects approximatel...
To assess with magnetoencephalography the developmental vs progressive character of the impairment o...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia (FRDA) is the most common autosomal recessive hereditary ataxia in Caucasians. N...
https://doi.org/10.1016/j.clinph.2019.10.021Friedreich ataxia (FRDA) is the most common recessive at...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia is the most frequent inherited ataxia in Caucasians. It is caused by deficiency ...
<div><p>Friedreich’s ataxia (FRDA) is a genetic neurodegenerative disorder caused by transcriptional...
AbstractFriedreich ataxia (FRDA) patients are homozygous for expanded GAA triplet-repeat alleles in ...
Friedreich’s ataxia (FRDA) is a rare genetic disorder caused by mutations in the gene frataxin, enco...
This magnetoencephalography (MEG) study addresses (i) how Friedreich ataxia (FRDA) affects the sub-s...
This magnetoencephalography (MEG) study addresses (i) how Friedreich ataxia (FRDA) affects the sub-s...
© 2011 Dr. Hamed AkhlaghiFriedreich ataxia (FRDA) is caused by mutations in the FXN gene leading to ...
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder that affects approximatel...
To assess with magnetoencephalography the developmental vs progressive character of the impairment o...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia (FRDA) is the most common autosomal recessive hereditary ataxia in Caucasians. N...
https://doi.org/10.1016/j.clinph.2019.10.021Friedreich ataxia (FRDA) is the most common recessive at...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia (FRDA) is a rare hereditary neurodegenerative disorder caused by a GAA repeat ex...
Friedreich's ataxia is the most frequent inherited ataxia in Caucasians. It is caused by deficiency ...
<div><p>Friedreich’s ataxia (FRDA) is a genetic neurodegenerative disorder caused by transcriptional...
AbstractFriedreich ataxia (FRDA) patients are homozygous for expanded GAA triplet-repeat alleles in ...
Friedreich’s ataxia (FRDA) is a rare genetic disorder caused by mutations in the gene frataxin, enco...