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Modeling and gene therapy of dysferlinopathyDysferlinopathies is a group of autosomal-recessive inherited neuromuscular diseases, which

Modeling and gene therapy of dysferlinopathyDysferlinopathies is a group of autosomal-recessive inherited neuromuscular diseases, which

Corrigendum: Twenty-year clinical progression of dysferlinopathy in patients from Dagestan [Front Neurol, 8, (2017) (77)] doi: 10.3389/fneur.2017.00077Corrigendum: Twenty-year clinical progression of dysferlinopathy in patients from Dagestan [Front

Twenty-year clinical progression of dysferlinopathy in patients from Dagestan been described. Dysferlinopathies are a form of limb-girdle muscle dystrophy type 2B with an incidence

Magnetic resonance imaging pattern variability in dysferlinopathy it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been

Corrigendum: Twenty-year clinical progression of dysferlinopathy in patients from Dagestan [Front Neurol, 8, (2017) (77)] doi: 10.3389/fneur.2017.00077Corrigendum: Twenty-year clinical progression of dysferlinopathy in patients from Dagestan [Front

RNA Editing for Muscular Dystrophy TherapyDysferlinopathy

Pre- and posttranscriptional genetic information modification in muscular dystrophy treatmentDysferlinopathy

Reactive Changes in Elements of Stromal-Vascular Differons of Dysferlin-Deficient Skeletal Muscles after Procaine Injectiondysferlinopathy

Twenty-year clinical progression of dysferlinopathy in patients from Dagestan been described. Dysferlinopathies are a form of limb-girdle muscle dystrophy type 2B with an incidence

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