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Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel

Crossref DOI link: https://doi.org/10.1186/s12881-016-0343-x

Published Online: 2016-11-16

Published Print: 2016-12

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

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