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
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