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.
Yamada K, Yuan J, Mano T, Takashima H, Shibata M
BMC Neurol. 2016 Oct 21; 16(1):201. PMID: 27765018.Abstract
