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Compound heterozygous patient with glycogen storage disease type III: Identification of two novel AGL mutations, a donor splice site mutation of Chinese origin and a 1-bp deletion of Japanese origin
✍ Scribed by Okubo, Minoru ;Horinishi, Asako ;Suzuki, Yoichi ;Murase, Toshio ;Hayasaka, Kiyoshi
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 148 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0148-7299
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