Whole-genome sequencing for mitochondrial disorders identifies unexpected mimics

Pract Neurol. 2023 Feb;23(1):2-3. doi: 10.1136/pn-2022-003570. Epub 2022 Oct 17.

Authors

Katherine R Schon^{1

2}, Patrick F Chinnery^{3

4}

Affiliations

¹ Department of Clinical Neurosciences, Cambridge Biomedical Campus, Cambridge, UK.
² Academic Department of Medical Genetics, Cambridge Biomedical Campus, Cambridge, UK.
³ Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK pfc25@cam.ac.uk.
⁴ MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK.

PMID: 36253087
DOI: 10.1136/pn-2022-003570

No abstract available

Keywords: genetics; mitochondrial disorders; neurogenetics.

Publication types

Editorial

MeSH terms

Humans
Mitochondrial Diseases* / diagnosis
Mitochondrial Diseases* / genetics
Sequence Analysis, DNA
Whole Genome Sequencing

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