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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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