Associated Papers
[Mitochondrial ornithine transporter deficiency].
Tsujino S et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine, 2002
A novel mutation, P126R, in a Japanese patient with HHH syndrome.
Miyamoto T et al.
Pediatric Neurology, 2002
[Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)].
Tsujino S et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine, 2001
Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X.
Miyamoto T et al.
Journal of Human Genetics, 2001
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