Search Results - "DeDionisio, Larry A."
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Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders
Published in Scientific reports (23-11-2017)“…CRISPR/Cas9 holds immense potential to treat a range of genetic disorders. Allele-specific gene disruption induced by non-homologous end-joining (NHEJ) DNA…”
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Journal Article -
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Mutation-Independent Allele-Specific Editing by CRISPR-Cas9, a Novel Approach to Treat Autosomal Dominant Disease
Published in Molecular therapy (05-08-2020)“…CRISPR-Cas9 provides a tool to treat autosomal dominant disease by non-homologous end joining (NHEJ) gene disruption of the mutant allele. In order to…”
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Late-onset lattice corneal dystrophy associated TGFBI p.H626R mutation in members of a Canadian family
Published in Canadian journal of ophthalmology (01-12-2019)Get full text
Journal Article