Friedreich ataxia
M Pandolfo - Neuromuscular Disorders of Infancy, Childhood, and …, 2015 - Elsevier
Friedreich's ataxia (FRDA) is the most common autosomal recessive hereditary ataxia in
Caucasians. Neurological symptoms dominate the clinical picture. The underlying …
Caucasians. Neurological symptoms dominate the clinical picture. The underlying …
[PDF][PDF] Friedreich Ataxia
M Pandolfo - John M. Walker, SERIES EDITOR - Citeseer
Friedreich ataxia (FA) is an autosomal-recessive disease primarily characterized by
progressive neurological disability. A significant proportion of patients also present with a …
progressive neurological disability. A significant proportion of patients also present with a …
Friedreich ataxia
M Pandolfo - Rosenberg's Molecular and Genetic Basis of …, 2020 - Elsevier
Friedreich ataxia (FRDA) is an autosomal-recessive disease characterized by progressive
neurological and cardiac abnormalities. It has a prevalence of around 2× 10 5 in persons of …
neurological and cardiac abnormalities. It has a prevalence of around 2× 10 5 in persons of …
Friedreich Ataxia
M Fry, K Usdin - Human Nucleotide Expansion Disorders, 2006 - Springer
Friedreich ataxia (FA) is the most common of the early-onset hereditary ataxias in Indo-
European and North African populations. The disease was first described in 1863 by …
European and North African populations. The disease was first described in 1863 by …
[PDF][PDF] Friedreich Ataxia
M Pandolfo - John M. Walker, SERIES EDITOR - researchgate.net
Friedreich ataxia (FA) is an autosomal-recessive disease primarily characterized by
progressive neurological disability. A significant proportion of patients also present with a …
progressive neurological disability. A significant proportion of patients also present with a …
[引用][C] Friedreich Ataxia
M Pandolfo - … Disorders of Infancy, Childhood, and Adolescence …, 2014 - difusion.ulb.ac.be
[PDF][PDF] Friedreich Ataxia
M Fry, K Usdin - Human Nucleotide Expansion Disorders, 2006 - ndl.ethernet.edu.et
Friedreich ataxia (FA) is the most common of the early-onset hereditary ataxias in Indo-
European and North African populations. The disease was first described in 1863 by …
European and North African populations. The disease was first described in 1863 by …
Friedreich Ataxia
M Pandolfo - Human Nucleotide Expansion Disorders - Springer
Friedreich ataxia (FA) is the most common of the early-onset hereditary ataxias in Indo-
European and North African populations. The disease was first described in 1863 by …
European and North African populations. The disease was first described in 1863 by …
[PDF][PDF] Friedreich Ataxia
M Pandolfo - John M. Walker, SERIES EDITOR - researchgate.net
Friedreich ataxia (FA) is an autosomal-recessive disease primarily characterized by
progressive neurological disability. A significant proportion of patients also present with a …
progressive neurological disability. A significant proportion of patients also present with a …
[PDF][PDF] Friedreich Ataxia
M Fry, K Usdin - Human Nucleotide Expansion Disorders, 2006 - ndl.ethernet.edu.et
Friedreich ataxia (FA) is the most common of the early-onset hereditary ataxias in Indo-
European and North African populations. The disease was first described in 1863 by …
European and North African populations. The disease was first described in 1863 by …