スポンサーリンク
Department of Neurology, Peking University First Hospital | 論文
- Reduction expression of thrombomodulin and endothelial cell nitric oxide synthase in dermatomyositis
- Hereditary sensory and autonomic neuropathy type I in a Chinese family : British C133W mutation exists in the Chinese
- Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes