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.2017.00077Umakhanova Z.,
Bardakov S.,
Mavlikeev M.,
Chernova O.,
Magomedova R.,
Akhmedova P.,
Yakovlev I.,
Dalgatov G.,
Fedotov V.,
Isaev A.,
Deev R. Corrigendum: Twenty-year clinical progression of
dysferlinopathy in patients from Dagestan [Front
Twenty-year clinical progression of dysferlinopathy in patients from DagestanUmakhanova Z.,
Bardakov S.,
Mavlikeev M.,
Chernova O.,
Magomedova R.,
Akhmedova P.,
Yakovlev I.,
Dalgatov G.,
Fedotov V.,
Isaev A.,
Deev R. been described.
Dysferlinopathies are a form of limb-girdle muscle dystrophy type 2B with an incidence
Magnetic resonance imaging pattern variability in dysferlinopathyBardakov S.N.,
Tsargush V.A.,
Carlier P.G.,
Nikitin S.S.,
Kurbatov S.A.,
Titova A.A.,
Umakhanova Z.R.,
Akhmedova P.G.,
Magomedova R.M.,
Zheleznyak I.S.,
Emelyantsev A.A.,
Berezhnaya E.N.,
A Yakovlev I.,
Isaev A.A.,
Deev R.V. 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.2017.00077Umakhanova Z.,
Bardakov S.,
Mavlikeev M.,
Chernova O.,
Magomedova R.,
Akhmedova P.,
Yakovlev I.,
Dalgatov G.,
Fedotov V.,
Isaev A.,
Deev R. Corrigendum: Twenty-year clinical progression of
dysferlinopathy in patients from Dagestan [Front
Twenty-year clinical progression of dysferlinopathy in patients from DagestanUmakhanova Z.,
Bardakov S.,
Mavlikeev M.,
Chernova O.,
Magomedova R.,
Akhmedova P.,
Yakovlev I.,
Dalgatov G.,
Fedotov V.,
Isaev A.,
Deev R. been described.
Dysferlinopathies are a form of limb-girdle muscle dystrophy type 2B with an incidence