Author

Mishan Britto

University of Warwick

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Benjamin Heath DurhamiD· 1 shared Margaret T. Lee· 1 shared Masanori MishimaiD· 1 shared Sandeep N. WontakaliD· 1 shared Sarah Tannenbaum· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

5 top collaborators · 10 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Benjamin Heath DurhamORCID

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1 paper

Recent·Most cited

A rare congenital anemia is caused by mutations in the centralspindlin complex

Sandeep N. Wontakal, Mishan Britto, Sarah Tannenbaum, Benjamin Heath Durham, Margaret T. Lee, Masanori Mishima

This study identifies compound heterozygous RACGAP1 variants causing CDAIII by disrupting the centralspindlin complex, leading to cytokinesis defects.

medRxiv · Apr 7, 2021 · PreprintGenetic & Genomic Medicine