First-line genomic diagnosis of mitochondrial disorders

F Lucy Raymond^{1

2

3}, Rita Horvath⁴, 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.

Comment

F Lucy Raymond et al. Nat Rev Genet. 2018 Jul.

. 2018 Jul;19(7):399-400.

doi: 10.1038/s41576-018-0022-1.

F Lucy Raymond^{1

2

3}, Rita Horvath⁴, Patrick F Chinnery^{5

6}

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.

No abstract available

Comment on

Paediatric genomics: diagnosing rare disease in children.
Wright CF, FitzPatrick DR, Firth HV. Wright CF, et al. Nat Rev Genet. 2018 May;19(5):253-268. doi: 10.1038/nrg.2017.116. Epub 2018 Feb 5. Nat Rev Genet. 2018. PMID: 29398702 Review.