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