AbstractMutations of SGCE encoding ε-sarcoglycan cause myoclonus-dystonia. SGCE is paternally expressed; however, 5–10% of patients show maternal inheritance of the disease. We found Sgce was exclusively paternally expressed in mice by using a novel polymorphism marker. The result was confirmed in Sgce heterozygous knockout mice. This finding suggests that maternally inherited myoclonus-dystonia may not result from maternal expression of SGCE. Furthermore, we report a new family of alternatively spliced Sgce mRNA expressed in the brain coding for different C-terminal sequences possessing a PDZ-binding motif. Our results provide a better basis for diagnosis and understanding of the pathogenesis of myoclonus-dystonia
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
Mutations of e-sarcoglycan gene (SGCE) have been implicated in myoclonus-dystonia (M-D), a movement ...
Mutations in the epsilon-sarcoglycan gene (SGCE) are associated with familial myoclonus dystonia, bu...
AbstractMutations of SGCE encoding ε-sarcoglycan cause myoclonus-dystonia. SGCE is paternally expres...
Loss-of-function mutations in SGCE, which encodes ε-sarcoglycan (ε-SG), cause myoclonus-dystonia syn...
Myoclonus-dystonia (M-D) is a movement disorder characterized by rapid muscle contractions and susta...
The dystonias are a common clinically and genetically heterogeneous group of movement disorders. Mor...
Myoclonus Dystonia (MD) is an autosomal dominant movement disorder characterized by bilateral myoclo...
Myoclonus-dystonia syndrome (MDS) is a non-degenerative neurological disorder that has been describe...
Myoclonus-dystonia syndrome (MDS) is a non-degenerative neurological disorder that has been describe...
Myoclonus-dystonia syndrome (MDS) is a non-degenerative neurological disorder that has been describe...
Myoclonus Dystonia (MD) is an autosomal dominant disease with high but incomplete penetrance and is ...
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
BACKGROUND: Myoclonus dystonia syndrome (MDS) is a hyperkinetic movement disorder caused, in a propo...
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
Mutations of e-sarcoglycan gene (SGCE) have been implicated in myoclonus-dystonia (M-D), a movement ...
Mutations in the epsilon-sarcoglycan gene (SGCE) are associated with familial myoclonus dystonia, bu...
AbstractMutations of SGCE encoding ε-sarcoglycan cause myoclonus-dystonia. SGCE is paternally expres...
Loss-of-function mutations in SGCE, which encodes ε-sarcoglycan (ε-SG), cause myoclonus-dystonia syn...
Myoclonus-dystonia (M-D) is a movement disorder characterized by rapid muscle contractions and susta...
The dystonias are a common clinically and genetically heterogeneous group of movement disorders. Mor...
Myoclonus Dystonia (MD) is an autosomal dominant movement disorder characterized by bilateral myoclo...
Myoclonus-dystonia syndrome (MDS) is a non-degenerative neurological disorder that has been describe...
Myoclonus-dystonia syndrome (MDS) is a non-degenerative neurological disorder that has been describe...
Myoclonus-dystonia syndrome (MDS) is a non-degenerative neurological disorder that has been describe...
Myoclonus Dystonia (MD) is an autosomal dominant disease with high but incomplete penetrance and is ...
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
BACKGROUND: Myoclonus dystonia syndrome (MDS) is a hyperkinetic movement disorder caused, in a propo...
The epsilon-sarcoglycan gene (SGCE) on human chromosome 7q21 has been reported to be a major locus f...
Mutations of e-sarcoglycan gene (SGCE) have been implicated in myoclonus-dystonia (M-D), a movement ...
Mutations in the epsilon-sarcoglycan gene (SGCE) are associated with familial myoclonus dystonia, bu...