Associated Papers
Hereditary Sensory and Autonomic Neuropathy Type 2: A Case Report and a Review of the Literature.
Ragucci C et al.
Brain Sciences, 2025
Rare diseases load through the study of a regional population.
Michel É et al.
Plos Genetics, 2025
41100445 (PubMed )
Supplement: pgen.1011876.s002.pdf
A novel mutation in the WNK1/HSN2 gene causing hereditary sensory and autonomic neuropathy type 2 in Chinese patient.
Ma S et al.
Journal of Human Genetics, 2025
WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study.
Yuan JH et al.
Clinical Genetics, 2017
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 et al.
Bmc Neurology, 2016
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