✦ LIBER ✦
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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