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TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy
CINRG Investigators
Neurology
Research output
:
Contribution to journal
›
Article
›
peer-review
32
Scopus citations
Overview
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Dive into the research topics of 'TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Duchenne Muscular Dystrophy
100%
Inborn Genetic Diseases
78%
Disease Progression
67%
Chromosomes, Human, Pair 1
41%
Whole Exome Sequencing
40%
Dystrophin
21%
Early Ambulation
21%
Phenotype
20%
Rare Diseases
16%
Walking
14%
Single Nucleotide Polymorphism
14%
Exons
14%
Genes
13%
Alleles
12%