Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients

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Authors: P. Laššuthová, R. Mazanec, D. Staněk, L. Sedláčková, B. Plevová, J. Haberlová, P. Seeman

Journal title: Scientific Reports

Journal number: 11

Journal publisher: Nature Publishing Group

Published year: 2022

DOI identifier: 10.1038/s41598-021-86857-0

ISSN: 2045-2322