A rare case of complete human erythrocyte AMP deaminase...

Human Mutation 2001 Vol. 17; Iss. 1

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

Yasukazu Yamada, Haruko Goto, Nobuaki Wakamatsu, Nobuaki Ogasawara
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Volume:
17
Year:
2001
Language:
english
Pages:
1
DOI:
10.1002/1098-1004(2001)17:13.0.co;2-b
File:
PDF, 39 KB
english, 2001
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