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Arthropathy-related pain in a patient with congenital impairment of pain sensation due to hereditary sensory and autonomic neuropathy type II with a rare mutation in the WNK1/HSN2 gene: a case report

Crossref DOI link: https://doi.org/10.1186/s12883-016-0727-8

Published Online: 2016-10-21

Published Print: 2016-12

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

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