A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3

✍ Scribed by Yasukazu Yamada; Haruko Goto; Nobuaki Wakamatsu; Nobuaki Ogasawara

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 39 KB
• Volume: 17
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/1098-1004(2001)17:1<78::aid-humu21>3.0.co;2-b