AbstractDystrophin is the recently discovered defective gene product in Duchenne and Becker muscular dystrophy (DMD and BMD). Dystrophin transcripts have been amplified and identified in diagnostic needle muscle biopsy samples using the polymerase chain reaction (PCR) procedure. Using 5′- and 3′-primers, dystrophin transcripts can be detected in both DMD and BMD muscle biopsies, on either side of defined deletions within the dystrophin gene
Progress in understanding the role of dystrophin raises promising hopes for a treatment for Duchenne...
Duchenne and Becker muscular dystrophies (DMD/BMD) are X-linked recessive neuromuscular disorders ca...
Duchenne/Becker muscular dystrophy (DMD/BMD) is an X-linked neuromuscular disease due to pathogenic ...
Mutations in the dystrophin gene result in both Duchenne and Becker muscular dystrophy (DMD and BMD)...
The dystrophin gene (DMD) is the largest gene in the human genome, mapping on the Xp21 chromosome lo...
Around 35% of Duchenne and Becker muscular dystrophy (DMD/BMD) patients cannot be identified by tech...
AbstractWe have examined the expression of several Duchenne muscular dystrophy (DMD) gene products i...
The dystrophin gene (DMD) is the largest gene in the human genome, mapping on the Xp21 chromosome lo...
Dystrophinopathy is the commonest form of muscular dystrophy and comprises clinically recognized for...
Clinical trials using strategies aimed at inducing dystrophin expression in Duchenne muscular dystro...
Duchenne muscular dystrophy (DMD) is the most prevalent inherited myopathy affecting children, cause...
Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder due to mutations i...
In recent years, the molecular understanding of human inherited disorders has been advanced by the i...
Duchenne Muscular Dystrophy (DMD) is one of a group of genetically heterogeneous muscular dystrophie...
International audienceDuchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caus...
Progress in understanding the role of dystrophin raises promising hopes for a treatment for Duchenne...
Duchenne and Becker muscular dystrophies (DMD/BMD) are X-linked recessive neuromuscular disorders ca...
Duchenne/Becker muscular dystrophy (DMD/BMD) is an X-linked neuromuscular disease due to pathogenic ...
Mutations in the dystrophin gene result in both Duchenne and Becker muscular dystrophy (DMD and BMD)...
The dystrophin gene (DMD) is the largest gene in the human genome, mapping on the Xp21 chromosome lo...
Around 35% of Duchenne and Becker muscular dystrophy (DMD/BMD) patients cannot be identified by tech...
AbstractWe have examined the expression of several Duchenne muscular dystrophy (DMD) gene products i...
The dystrophin gene (DMD) is the largest gene in the human genome, mapping on the Xp21 chromosome lo...
Dystrophinopathy is the commonest form of muscular dystrophy and comprises clinically recognized for...
Clinical trials using strategies aimed at inducing dystrophin expression in Duchenne muscular dystro...
Duchenne muscular dystrophy (DMD) is the most prevalent inherited myopathy affecting children, cause...
Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder due to mutations i...
In recent years, the molecular understanding of human inherited disorders has been advanced by the i...
Duchenne Muscular Dystrophy (DMD) is one of a group of genetically heterogeneous muscular dystrophie...
International audienceDuchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caus...
Progress in understanding the role of dystrophin raises promising hopes for a treatment for Duchenne...
Duchenne and Becker muscular dystrophies (DMD/BMD) are X-linked recessive neuromuscular disorders ca...
Duchenne/Becker muscular dystrophy (DMD/BMD) is an X-linked neuromuscular disease due to pathogenic ...