INTRODUCTION: Calpain 3 deficiency causes limb girdle muscular dystrophy type 2A, which is one of the most common forms of limb girdle muscular dystrophy. Nevertheless, calpainopathy is not always associated with mutations in the specific gene and secondary reduction in protein expression has been described. CASE REPORT: We report a case of a 43-year-old man who complained of thigh muscle stiffness and had muscle hypertrophy of both vastus medialis with prolonged myotonic contraction by percussion. A muscle biopsy showed dystrophic features and calpain 3 deficiency was shown by immunoblot analysis although mutations in the specific gene were not found. Known cases of secondary calpain 3 protein deficiency were ruled out and mutations in MD...
AbstractLimb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic eti...
Objective: To determine the frequency of calpain III mutations in a heterogeneous limb-girdle muscul...
The autosomal recessive limb-girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in th...
INTRODUCTION: Calpain 3 deficiency causes limb girdle muscular dystrophy type 2A, which is one of th...
Introduction: Calpain 3 deficiency causes limb girdle muscular dystrophy type 2A, which is one of th...
Limb girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in the calpain 3 gene. In a l...
International audienceRecessively inherited limb girdle muscular dystrophy (LGMD) type 2A is the mos...
<p>The clinical presentation of progressive limb-girdle muscular dystrophy type 2A (LGMD2A) is due t...
Background: Limb girdle muscular dystrophy (LGMD) type 2A is caused by mutations in the CAPN3 gene a...
AbstractLimb girdle muscular dystrophy type 2A results from mutations in the gene encoding the calpa...
Limb girdle muscular dystrophy type 2A results from mutations in the gene encoding the calpain 3 pro...
Dysferlin is the protein product of the gene (DYSF) that is defective in patients with limb girdle m...
Limb-girdle muscular dystrophy type 2A (LGMD2A) is an autosomal recessive disorder characterized by ...
Calpainopathy (LGMD2A) is the most common type of autosomal recessive limb-girdle muscular dystrophy...
Limb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic etiology ha...
AbstractLimb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic eti...
Objective: To determine the frequency of calpain III mutations in a heterogeneous limb-girdle muscul...
The autosomal recessive limb-girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in th...
INTRODUCTION: Calpain 3 deficiency causes limb girdle muscular dystrophy type 2A, which is one of th...
Introduction: Calpain 3 deficiency causes limb girdle muscular dystrophy type 2A, which is one of th...
Limb girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in the calpain 3 gene. In a l...
International audienceRecessively inherited limb girdle muscular dystrophy (LGMD) type 2A is the mos...
<p>The clinical presentation of progressive limb-girdle muscular dystrophy type 2A (LGMD2A) is due t...
Background: Limb girdle muscular dystrophy (LGMD) type 2A is caused by mutations in the CAPN3 gene a...
AbstractLimb girdle muscular dystrophy type 2A results from mutations in the gene encoding the calpa...
Limb girdle muscular dystrophy type 2A results from mutations in the gene encoding the calpain 3 pro...
Dysferlin is the protein product of the gene (DYSF) that is defective in patients with limb girdle m...
Limb-girdle muscular dystrophy type 2A (LGMD2A) is an autosomal recessive disorder characterized by ...
Calpainopathy (LGMD2A) is the most common type of autosomal recessive limb-girdle muscular dystrophy...
Limb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic etiology ha...
AbstractLimb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic eti...
Objective: To determine the frequency of calpain III mutations in a heterogeneous limb-girdle muscul...
The autosomal recessive limb-girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in th...