✦ LIBER ✦
Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X
✍ Scribed by T. Miyamoto; N. Kanazawa; S. Kato; M. Kawakami; Y. Inoue; T. Kuhara; T. Inoue; K. Takeshita; S. Tsujino
- Publisher
- Nature Publishing Group
- Year
- 2001
- Tongue
- English
- Weight
- 62 KB
- Volume
- 46
- Category
- Article
- ISSN
- 1435-232X
No coin nor oath required. For personal study only.