A relatively common cause of hereditary motor neuropathy due to a founder mutation in VWA1 (2023)

First Author: Nagy S.

Attributed to: MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases funded by MRC

No abstract provided

Type: Conference/Paper/Proceeding/Abstract

Volume: 30

Parent Publication: EUROPEAN JOURNAL OF NEUROLOGY

ISSN: 1351-5101