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Number of items: 3.

Article

Storey, E and Fuller, HR ORCID: https://orcid.org/0000-0001-8868-896X (2022) Genotype-phenotype correlations in human diseases caused by mutations of LINC complex-associated genes: a systematic review and meta-summary. Cells, 11 (24).

Storey, E and Fuller, HR ORCID: https://orcid.org/0000-0001-8868-896X (2022) Genotype-phenotype correlations in human diseases caused by mutations of LINC complex-associated genes: a systematic review and meta-summary. Neuromuscular Disorders, 32 (S1).

Conference or Workshop Item

Storey, E, Holt, I, Owen, S, Synowsky, S, Shirran, S, Morris, G and Fuller, HR ORCID: https://orcid.org/0000-0001-8868-896X (2022) Characterising the molecular consequences of LMNA-related congenital muscular dystrophy in patient myoblasts. In: 27th International Hybrid Annual Congress of the World Muscle Society, 11-15 Oct 2022, Halifax, Nova Scotia, Canada.

This list was generated on Wed Nov 1 01:38:44 2023 UTC.