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
3 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献