Demyelination in hereditary sensory neuropathy type‐1C
Annals of Clinical and Translational Neurology2020Vol. 7(9), pp. 1502–1512
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Abstract
Mutations in the SPTLC2 cause a demyelinating phenotype resembling those in acquired demyelinating polyneuropathy. The species of increased DoxSLs in HSN1C may be more diverse than originally thought.
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