Associated Papers
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
Hereditary sensory and autonomic neuropathy II due to novel mutation in the HSN2 gene in Mexican families.
Pacheco-Cuellar G et al.
Journal of Neurology, 2011
New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2.
Takagi M et al.
Neurology, 2006
Novel mutation in the HSN2 gene in a Korean patient with hereditary sensory and autonomic neuropathy type 2.
Cho HJ et al.
Journal of Human Genetics, 2006
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