Pseudoexon activation increases phenotype severity in a Becker muscular dystrophy patient.
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Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study.Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies.Lessons from non-canonical splicingTranslational development of splice-modifying antisense oligomers.Deep intronic mutations and human disease.Normal and altered pre-mRNA processing in the DMD gene.Detailed molecular characterization of a novel IDS exonic mutation associated with multiple pseudoexon activation.
P2860
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P2860
Pseudoexon activation increases phenotype severity in a Becker muscular dystrophy patient.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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name
Pseudoexon activation increase ...... er muscular dystrophy patient.
@ast
Pseudoexon activation increase ...... er muscular dystrophy patient.
@en
type
label
Pseudoexon activation increase ...... er muscular dystrophy patient.
@ast
Pseudoexon activation increase ...... er muscular dystrophy patient.
@en
prefLabel
Pseudoexon activation increase ...... er muscular dystrophy patient.
@ast
Pseudoexon activation increase ...... er muscular dystrophy patient.
@en
P2093
P2860
P356
P1476
Pseudoexon activation increase ...... er muscular dystrophy patient.
@en
P2093
Aileen Reghan Foley
Bryan J Lynch
Emily Rice
Eoin O Rathallaigh
Kane Greer
Kayla Mizzi
Lukas Kuster
Matthew I Bellgard
Roberto A Barrero
Steve D Wilton
P2860
P304
P356
10.1002/MGG3.144
P577
2015-04-15T00:00:00Z