✦ LIBER ✦
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation
✍ Scribed by R. Spiegel; A. Shaag; A. Gutman; S. H. Korman; A. Saada; O. Elpeleg; S. A. Shalev
- Book ID
- 106374196
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 126 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0141-8955
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