Perils of predictive testing for unaffected people from motor neuron disease families with no identified causal gene
Amyotroph Lateral Scler Frontotemporal Degener
.
2024 Dec 9:1-2.
doi: 10.1080/21678421.2024.2438153.
Online ahead of print.
Authors
Alisdair Mcneill
1
2
,
Andrew G L Douglas
3
4
,
Rhona Macleod
5
6
,
Nayana Lahiri
7
;
UK PREDICTIVE NEUROGENETICS TESTING CONSORTIUM
Affiliations
1
Division of Neuroscience, the University of Sheffield, Sheffield, UK.
2
Sheffield Clinical Genetics Service, Sheffield Children's Hospital NHS Foundation Trust, Sheffield, UK.
3
Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
4
Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
5
Division of Evolution, Infection and Genomics, School of Biological Sciences, The University of Manchester, Manchester, UK.
6
Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester, UK.
7
Department of Clinical Genetics, St George's University Hospitals NHS Foundation Trust, South West Thames Centre for Genomics, London, UK.
PMID:
39648759
DOI:
10.1080/21678421.2024.2438153
No abstract available