Screening for genetic mutations in patients with neuropathy without definite etiology is useful
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-020-09899-w.pdf
Reference14 articles.
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3. Adams D et al (2018) Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis. N Engl J Med 379(1):11–21
4. Cortese A et al (2020) Targeted next-generation sequencing panels in the diagnosis of Charcot–Marie–Tooth disease. Neurology 94(1):e51–e61
5. Magrinelli F et al (2020) Pharmacological treatment for familial amyloid polyneuropathy. Cochrane Database Syst Rev 4:CD012395
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