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Genetic, structural, and functional analysis of mutations causing methylmalonyl-CoA epimerase deficiency


Heuberger, Kathrin; Bailey, Henry J; Burda, Patricie; Chaikuad, Apirat; Krysztofinska, Ewelina; Suormala, Terttu; Bürer, Céline; Lutz, Seraina; Fowler, Brain; Froese, D Sean; Yue, Wyatt W; Baumgartner, Matthias R (2018). Genetic, structural, and functional analysis of mutations causing methylmalonyl-CoA epimerase deficiency. bioRxiv 484048, University of Zurich.

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Item Type:Working Paper
Communities & Collections:04 Faculty of Medicine > University Children's Hospital Zurich > Medical Clinic
Dewey Decimal Classification:610 Medicine & health
Language:English
Date:2018
Deposited On:31 Jan 2020 13:25
Last Modified:29 Jul 2020 13:11
Series Name:bioRxiv
OA Status:Green
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1101/484048

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