WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study
J.‐H. Yuan; A. Hashiguchi; A. Yoshimura; N. Sakai; M.P. Takahashi; T. Ueda; A. Taniguchi; S. Okamoto; N. Kanazawa; Y. Yamamoto; K. Saigoh; S. Kusunoki; M. Ando; Y. Hiramatsu; Y. Okamoto; H. Takashima
Author Information: Department of Neurology and Geriatrics
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