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

PubMed Identifier: 34732400

Publication URI: http://europepmc.org/abstract/MED/34732400

Type: Journal Article/Review

Volume: 375

Parent Publication: BMJ (Clinical research ed.)

ISSN: 0959-8138