Add to ORKGCentronuclear myopathy (CNM) is a rare congenital disorder of striated muscle. It is characterized pathologically by a high frequency of central nuclei in the muscle fibers.1 Mutations in the gene encoding myotubularinare responsible for the X
Centronuclear myopathy (CNM) is a slowly progressive congenital myopathy characterized by abnormal c...
BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuc...
Centronucleus myopathy is a group of congenital myopathy,with the pathological features of the locat...
International audienceCentronuclear myopathy (CNM) is an inherited neuromuscular disorder characteri...
Centronuclear myopathy (CNM) is a genetically heterogeneous congenital myopathy characterized by mus...
Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein ...
Abstract Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinic...
Contains fulltext : 182290.pdf (publisher's version ) (Closed access)Autosomal dom...
Centronuclear myopathies (CNM) are a clinically and genetically heterogeneous group of congenital my...
Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein ...
Centronuclear myopathy (CNM) is a group of rare genetic muscle disorders characterized by muscle fib...
Centronuclear myopathies (CNM) are rare congenital disorders characterized by muscle weakness and st...
Centronuclear myopathies (CNM) are a group of diseases with variable onset and severity sharing as a...
© 2017 Elsevier B.V. Centronuclear myopathies (CNM) are a clinically and genetically heterogeneous g...
BackgroundzzCentral core disease (CCD) is a congenital myopathy characterized by distinc-tive cores ...
Centronuclear myopathy (CNM) is a slowly progressive congenital myopathy characterized by abnormal c...
BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuc...
Centronucleus myopathy is a group of congenital myopathy,with the pathological features of the locat...
International audienceCentronuclear myopathy (CNM) is an inherited neuromuscular disorder characteri...
Centronuclear myopathy (CNM) is a genetically heterogeneous congenital myopathy characterized by mus...
Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein ...
Abstract Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinic...
Contains fulltext : 182290.pdf (publisher's version ) (Closed access)Autosomal dom...
Centronuclear myopathies (CNM) are a clinically and genetically heterogeneous group of congenital my...
Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein ...
Centronuclear myopathy (CNM) is a group of rare genetic muscle disorders characterized by muscle fib...
Centronuclear myopathies (CNM) are rare congenital disorders characterized by muscle weakness and st...
Centronuclear myopathies (CNM) are a group of diseases with variable onset and severity sharing as a...
© 2017 Elsevier B.V. Centronuclear myopathies (CNM) are a clinically and genetically heterogeneous g...
BackgroundzzCentral core disease (CCD) is a congenital myopathy characterized by distinc-tive cores ...
Centronuclear myopathy (CNM) is a slowly progressive congenital myopathy characterized by abnormal c...
BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuc...
Centronucleus myopathy is a group of congenital myopathy,with the pathological features of the locat...