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Activating internal ribosome entry to treat Duchenne muscular dystrophy
British Library Online Contents | 2014| -
P1.41 Recurrent mutations in TPM3 likely arise from gene conversion events linked to multiple Tm5NM1 pseudogenes in the genome
British Library Online Contents | 2010| -
Therapeutics for Childhood Neurofibromatosis Type 1 and Type 2
British Library Online Contents | 2011| -
ACTN3: A Genetic Influence on Muscle Function and Athletic Performance
British Library Online Contents | 2007| -
S.P.53 Interventions for increasing ankle flexibility in patients with neuromuscular disease: A Cochrane Systematic Review
British Library Online Contents | 2012| -
The evolution of skeletal muscle performance: gene duplication and divergence of human sarcomeric a-actinins
British Library Online Contents | 2010| -
A gene for speed? The evolution and function of alpha-actinin-3
British Library Online Contents | 2004| -
Relationship between foot strength and motor function in preschool-age children
British Library Online Contents | 2009| -
Can in-the-moment diary methods measure health-related quality of life in Duchenne muscular dystrophy?
British Library Online Contents | 2017| -
Visual-evoked potentials in the assessment of optic gliomas
British Library Online Contents | 2001| -
Developmental delay expressive aphasia, hypotonia and dysmorphism in two brothers: an X-linked mental retardation syndrome?
British Library Online Contents | 1998| -
External ophthalmoplegia in neuromuscular disorders: case report and review of the literature
British Library Online Contents | 1997| -
Recent advances in diagnosis of the childhood muscular dystrophies
British Library Online Contents | 1997| -
How does α-actinin-3 deficiency alter muscle function? Mechanistic insights into ACTN3, the ‘gene for speed’
British Library Online Contents | 2016|
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