International audienceDysferlinopathies are a group of autosomal recessive muscular dystrophies caused by mutations in the dysferlin gene. This study presents clinical features and the mutational spectrum in the largest cohort of Chinese patients analyzed to date
Mutations in the fukutin-related protein (FKRP) gene have been associated with dystroglycanopathies,...
International audienceDYSF encoding dysferlin is mutated in Miyoshi myopathy and Limb-Girdle Muscula...
Inherited muscular disorders (IMDs) are clinically and genetically heterogeneous genetic disorders. ...
International audienceDysferlinopathies are a group of autosomal recessive muscular dystrophies caus...
International audienceDysferlinopathies belong to the heterogeneous group of autosomal recessive mus...
Background: Dysferlinopathy is caused by mutations in the dysferlin (DYSF) gene. Here, we described ...
Dysferlinopathy refers to autosomal recessive muscular dystrophies caused by mutations in dysferlin ...
Aims Dysferlinopathy is an autosomal recessive muscular dystrophy, caused by bi-allelic variants ...
Objective To investigate clinical phenotype and gene mutation of dysferlinopathy. Methods The clinic...
BACKGROUND: Dysferlin is reduced in patients with limb girdle muscular dystrophy type 2B, Miyoshi my...
Dysferlinopathy is an autosomal recessive muscular dystrophy, caused by bi-allelic variants in the g...
Abstract Background Dystrophinopathies are a set of severe and incurable X-linked neuromuscular diso...
Background: Facioscapulohumeral muscular dystrophy (FSHD), a common autosomal dominant muscular diso...
Dysferlinopathies encompass a large variety of neuromuscular diseases characterized by the absence o...
Mutations in the gene encoding dysferlin cause limb girdle muscular dystrophy type 2B and distal Miy...
Mutations in the fukutin-related protein (FKRP) gene have been associated with dystroglycanopathies,...
International audienceDYSF encoding dysferlin is mutated in Miyoshi myopathy and Limb-Girdle Muscula...
Inherited muscular disorders (IMDs) are clinically and genetically heterogeneous genetic disorders. ...
International audienceDysferlinopathies are a group of autosomal recessive muscular dystrophies caus...
International audienceDysferlinopathies belong to the heterogeneous group of autosomal recessive mus...
Background: Dysferlinopathy is caused by mutations in the dysferlin (DYSF) gene. Here, we described ...
Dysferlinopathy refers to autosomal recessive muscular dystrophies caused by mutations in dysferlin ...
Aims Dysferlinopathy is an autosomal recessive muscular dystrophy, caused by bi-allelic variants ...
Objective To investigate clinical phenotype and gene mutation of dysferlinopathy. Methods The clinic...
BACKGROUND: Dysferlin is reduced in patients with limb girdle muscular dystrophy type 2B, Miyoshi my...
Dysferlinopathy is an autosomal recessive muscular dystrophy, caused by bi-allelic variants in the g...
Abstract Background Dystrophinopathies are a set of severe and incurable X-linked neuromuscular diso...
Background: Facioscapulohumeral muscular dystrophy (FSHD), a common autosomal dominant muscular diso...
Dysferlinopathies encompass a large variety of neuromuscular diseases characterized by the absence o...
Mutations in the gene encoding dysferlin cause limb girdle muscular dystrophy type 2B and distal Miy...
Mutations in the fukutin-related protein (FKRP) gene have been associated with dystroglycanopathies,...
International audienceDYSF encoding dysferlin is mutated in Miyoshi myopathy and Limb-Girdle Muscula...
Inherited muscular disorders (IMDs) are clinically and genetically heterogeneous genetic disorders. ...