Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study. (2021)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
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