Giddings John | 奈良県立医科大学 小児科学
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概要
奈良県立医科大学 小児科学 | 論文
- Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X
- A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease) : molecular genetic study
- Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
- Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis