Two families with spinocerebellar ataxia type 7 are presented. Although there are affected cousins, it is not the sibling parents that transmitted the mutation. It is assumed that the affected families share a common ancestor
Spinocerebellar Ataxia Type 7 (SCA7) is an autosomal dominant disorder associated with progressive v...
Spinocerebellar ataxias are classified according to the clinical signs, affected neuroanatomical reg...
The spinocerebellar ataxias (SCA) are a group of neurodegenerative disorders cha...
Two families with spinocerebellar ataxia type 7 are presented. Although there are affected cousins, ...
Copyright © 2014 F. Zaheer and D. Fee.This is an open access article distributed under the Creative ...
Over the past five years, rapid progress has been made in genetically identifying dif-ferent forms o...
Spinocerebellar ataxia (SCA) types 2 and 3 are autosomal-dominant neurodegenerative disorders caused...
Aim of the study: To report a family with a novel TRIO gene mutation associated withphenotype of cer...
Spinocerebellar ataxia type 7 (SCA7) is a hereditary neurodegenerative disorder affecting the cerebe...
Background: To date, 43 types of Spinocerebellar Ataxias (SCAs) have been identified. A subset of th...
Aim of the study. Multiple system atrophy (MSA) and spinocerebellar ataxia (SCA) share similar sympt...
OBJECTIVE: To compare the clinical and genetic features of the seven-generation family (MN-A) used t...
Introduction. We present the first two Polish families diagnosed with spinocerebellar ataxia type 7 ...
Journal ArticleThe gene for spinocerebellar ataxia 7 (SCA7) includes a transcribed, translated CAG t...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...
Spinocerebellar Ataxia Type 7 (SCA7) is an autosomal dominant disorder associated with progressive v...
Spinocerebellar ataxias are classified according to the clinical signs, affected neuroanatomical reg...
The spinocerebellar ataxias (SCA) are a group of neurodegenerative disorders cha...
Two families with spinocerebellar ataxia type 7 are presented. Although there are affected cousins, ...
Copyright © 2014 F. Zaheer and D. Fee.This is an open access article distributed under the Creative ...
Over the past five years, rapid progress has been made in genetically identifying dif-ferent forms o...
Spinocerebellar ataxia (SCA) types 2 and 3 are autosomal-dominant neurodegenerative disorders caused...
Aim of the study: To report a family with a novel TRIO gene mutation associated withphenotype of cer...
Spinocerebellar ataxia type 7 (SCA7) is a hereditary neurodegenerative disorder affecting the cerebe...
Background: To date, 43 types of Spinocerebellar Ataxias (SCAs) have been identified. A subset of th...
Aim of the study. Multiple system atrophy (MSA) and spinocerebellar ataxia (SCA) share similar sympt...
OBJECTIVE: To compare the clinical and genetic features of the seven-generation family (MN-A) used t...
Introduction. We present the first two Polish families diagnosed with spinocerebellar ataxia type 7 ...
Journal ArticleThe gene for spinocerebellar ataxia 7 (SCA7) includes a transcribed, translated CAG t...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...
Spinocerebellar Ataxia Type 7 (SCA7) is an autosomal dominant disorder associated with progressive v...
Spinocerebellar ataxias are classified according to the clinical signs, affected neuroanatomical reg...
The spinocerebellar ataxias (SCA) are a group of neurodegenerative disorders cha...
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