The DMD gene is the largest in the human genome, with a total intron content exceeding 2.2Mb. In the decades since DMD was discovered there have been numerous reported cases of pseudoexons (PEs) arising in the mature DMD transcripts of some individuals, either as the result of mutations or as low-frequency errors of the spliceosome. In this review, I collate from the literature 58 examples of DMD PEs and examine the diversity and commonalities of their features. In particular, I note the high frequency of PEs that arise from deep intronic SNVs and discuss a possible link between PEs induced by distal mutations and the regulation of recursive splicing
Objective: Dysferlin is a large transmembrane protein that functions in critical processes of membra...
Duchenne muscular dystrophy is an inherited muscle wasting disease with severe symptoms and onset in...
A Becker muscular dystrophy patient was found to have a single base substitution at the 5' end of in...
DMD is the largest gene in the human genome, spanning over 2.2Mb of the X chromosome, and more than ...
We report a dystrophinopathy patient with an in-frame deletion of DMD exons 45–47, and therefore a g...
Understanding pre-mRNA splicing is crucial to accurately diagnosing and treating genetic diseases. H...
We report a dystrophinopathy patient with an in‐frame deletion of DMD exons 45–47, and therefore a g...
L'épissage des ARN pré-messagers est une étape essentielle pour l'expression des gènes chez les euca...
We describe two donor splice site mutations, affecting dystrophin exons 16 and 45 that led to Duchen...
DMD nonsense and frameshift mutations lead to severe Duchenne muscular dystrophy while in-frame muta...
Background: The dystrophin gene is the one of the largest described in human beings and mutations as...
International audienceWe have analysed the splicing pattern of the human Duchenne Muscular Dystrophy...
AbstractThe mechanisms by which huge human introns are spliced out precisely are poorly understood. ...
We present the case of a male patient who was ultimately diagnosed with Becker muscular dystrophy (B...
Duchenne muscular dystrophy (DMD) is a severe muscular disorder. It was reported that multiple exon ...
Objective: Dysferlin is a large transmembrane protein that functions in critical processes of membra...
Duchenne muscular dystrophy is an inherited muscle wasting disease with severe symptoms and onset in...
A Becker muscular dystrophy patient was found to have a single base substitution at the 5' end of in...
DMD is the largest gene in the human genome, spanning over 2.2Mb of the X chromosome, and more than ...
We report a dystrophinopathy patient with an in-frame deletion of DMD exons 45–47, and therefore a g...
Understanding pre-mRNA splicing is crucial to accurately diagnosing and treating genetic diseases. H...
We report a dystrophinopathy patient with an in‐frame deletion of DMD exons 45–47, and therefore a g...
L'épissage des ARN pré-messagers est une étape essentielle pour l'expression des gènes chez les euca...
We describe two donor splice site mutations, affecting dystrophin exons 16 and 45 that led to Duchen...
DMD nonsense and frameshift mutations lead to severe Duchenne muscular dystrophy while in-frame muta...
Background: The dystrophin gene is the one of the largest described in human beings and mutations as...
International audienceWe have analysed the splicing pattern of the human Duchenne Muscular Dystrophy...
AbstractThe mechanisms by which huge human introns are spliced out precisely are poorly understood. ...
We present the case of a male patient who was ultimately diagnosed with Becker muscular dystrophy (B...
Duchenne muscular dystrophy (DMD) is a severe muscular disorder. It was reported that multiple exon ...
Objective: Dysferlin is a large transmembrane protein that functions in critical processes of membra...
Duchenne muscular dystrophy is an inherited muscle wasting disease with severe symptoms and onset in...
A Becker muscular dystrophy patient was found to have a single base substitution at the 5' end of in...