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A Japanese boy with adenine phosphoribosyltransferase (APRT) deficiency caused by compound heterozygosity including a novel missense mutation in APRT gene

✍ Scribed by Hiroki Nozue; Tomohiro Kamoda; Hisako Saitoh; Kunio Ichikawa; Atsuo Taniguchi


Book ID
114817071
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
314 KB
Volume
100
Category
Article
ISSN
0803-5253

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