Author: "Storey, E." / Journal: neuromuscular disorders - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Storey, E."' showing total 6 results

Start Over Author "Storey, E." Journal neuromuscular disorders

6 results on '"Storey, E."'

1. P.146 Characterising the molecular consequences of LMNA-related congenital muscular dystrophy in patient myoblasts

Author: Storey, E., primary, Holt, I., additional, Owen, S., additional, Synowsky, S., additional, Shirran, S., additional, Morris, G., additional, and Fuller, H., additional
Published: 2022
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2. P.148 Genotype-phenotype correlations in human diseases caused by mutations of LINC complex-associated genes: a systematic review and meta-summary

Author: Storey, E., primary and Fuller, H., additional
Published: 2022
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3. OTHER NMDs

Author: Storey, E., primary, Holt, I., additional, Morris, G., additional, and Fuller, H., additional
Published: 2021
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4. CONGENITAL MUSCULAR DYSTROPHIES

Author: Storey, E., primary, Khilar, S., additional, Holt, I., additional, Shirran, S., additional, Morris, G., additional, and Fuller, H., additional
Published: 2021
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5. OTHER NMDs: EP.350 A study of LINC complex proteins reveals temporal emerin and SUN2 expression changes during myoblast differentiation

Author: Storey, E., Holt, I., Morris, G., and Fuller, H.
Published: 2021
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6. CONGENITAL MUSCULAR DYSTROPHIES: EP.66 Identification of lamin A interactors in healthy and congenital muscular dystrophy immortalized myoblasts

Author: Storey, E., Khilar, S., Holt, I., Shirran, S., Morris, G., and Fuller, H.
Published: 2021
Full Text: View/download PDF

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