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Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity

✍ Scribed by M. Staudt; B. Wermuth; P. Freisinger; A. Hässler; B. F. Pontz


Book ID
110222678
Publisher
Springer
Year
1998
Tongue
English
Weight
119 KB
Volume
21
Category
Article
ISSN
0141-8955

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