Affiliation:
1. Department of Biomedical Sciences School of Biology and Medicine University of Lausanne, Lausanne Switzerland
Abstract
This scientific commentary refers to ‘Bi-allelic truncating mutations in VWA1 cause neuromyopathy’, by Deschauer et al. (doi:10.1093/brain/awaa418) and ‘An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy’, by Pagnamenta et al. (doi:10.1093/brain/awaa420)
Publisher
Oxford University Press (OUP)
Cited by
2 articles.
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