Ambivalence and regret in genome sequencing

Alisdair McNeill^{1

2}

Affiliations

¹ Division of Neuroscience, The University of Sheffield, Sheffield, UK. a.mcneill@sheffield.ac.uk.
² Sheffield Clinical Genetics Department, Sheffield Children's Hospital NHS Foundation Trust, Sheffield, UK. a.mcneill@sheffield.ac.uk.

Editorial

Alisdair McNeill. Eur J Hum Genet. 2023 Dec.

. 2023 Dec;31(12):1343.

doi: 10.1038/s41431-023-01491-w.

Alisdair McNeill^{1

2}

¹ Division of Neuroscience, The University of Sheffield, Sheffield, UK. a.mcneill@sheffield.ac.uk.
² Sheffield Clinical Genetics Department, Sheffield Children's Hospital NHS Foundation Trust, Sheffield, UK. a.mcneill@sheffield.ac.uk.

No abstract available

Conflict of interest statement

The author declares no competing interests.

A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy.
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