Document is current

Any future updates will be listed below

An axonal Charcot–Marie–Tooth disease associated with a homozygous GDAP1 gene mutation in two siblings from Bangladesh: a less severe phenotype

Crossref DOI link: https://doi.org/10.1007/s13760-022-01884-6

Published Online: 2022-03-22

Published Print: 2022-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

About CrossMark