First-line genomic diagnosis of mitochondrial disorders
Nat Rev Genet
.
2018 Jul;19(7):399-400.
doi: 10.1038/s41576-018-0022-1.
Authors
F Lucy Raymond
1
2
3
,
Rita Horvath
4
,
Patrick F Chinnery
5
6
Affiliations
1
NIHR Translational BioResource in Common and Rare Diseases, University of Cambridge, Cambridge, UK.
2
Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.
3
Department of Medical Genetics, University of Cambridge, Cambridge, UK.
4
Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
5
NIHR Translational BioResource in Common and Rare Diseases, University of Cambridge, Cambridge, UK. pfc25@cam.ac.uk.
6
Department of Clinical Neurosciences and MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK. pfc25@cam.ac.uk.
PMID:
29789687
DOI:
10.1038/s41576-018-0022-1
No abstract available
Publication types
Research Support, Non-U.S. Gov't
Comment
MeSH terms
Child
Genomics
Humans
Mitochondrial Diseases*
Rare Diseases*
Grants and funding
MR/N025431/1/MRC_/Medical Research Council/United Kingdom
MR/N010035/1/MRC_/Medical Research Council/United Kingdom
MC_UP_1501/2/MRC_/Medical Research Council/United Kingdom
G1000848/MRC_/Medical Research Council/United Kingdom
MR/N025431/2/MRC_/Medical Research Council/United Kingdom
G0601943/MRC_/Medical Research Council/United Kingdom