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HARVARD Citation
Yuan, J. et al. (2017). WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study. Clinical genetics. 92 (6), pp. 659-663. [Online].
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Yuan, J. et al. (2017). WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study. Clinical genetics. 92 (6), pp. 659-663. [Online].