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Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study (2021)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/bmj-2021-066288

Publication URI: http://dx.doi.org/10.1136/bmj-2021-066288

Type: Journal Article/Review

Parent Publication: BMJ