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Lianne Abbott

UCL Institute of Child Health

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Duchenne muscular dystrophy patients lacking the dystrophin isoforms Dp140 and Dp71 and mouse models lacking Dp140 have a more severe motor phenotype

2021 medRxiv
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Characterising the Influence of Dystrophin Brain Isoform Involvement on the Pattern of Motor Impairment in Duchenne Muscular Dystrophy (4467)

2021 Neurology
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Longitudinal changes in respiratory and upper limb function in a pediatric type III spinal muscular atrophy cohort after loss of ambulation.

2021 Muscle & Nerve
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