Are the UK genetic testing criteria for dementia too exclusive?
Author:
Funder
National Institute for Health Research
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-021-10867-1.pdf
Reference15 articles.
1. Lefroy H, Harrison V, Németh AH (2020) Genetic testing in neurology. Medicine 48(8):545–549
2. Coyle-Gilchrist IT, Dick KM, Patterson K et al (2016) Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes. Neurology 86(18):1736–1743
3. Rohrer J, Guerreiro R, Vandrovcova J et al (2009) The heritability and genetics of frontotemporal lobar degeneration. Neurology 73(18):1451–1456
4. Greaves CV, Rohrer JD (2019) An update on genetic frontotemporal dementia. J Neurol 266(8):2075–2086
5. DeJesus-Hernandez M, Mackenzie IR, Boeve BF et al (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72(2):245–256
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