✦ LIBER ✦
Infantile mitochondrial DNA depletion syndrome associated with methylmalonic aciduria and 3-methylcrotonyl-CoA and propionyl-CoA carboxylase deficiencies in two unrelated patients: A new phenotype of mtDNA depletion syndrome
✍ Scribed by S. Yano; L. Li; T. P. Le; K. Moseley; A. Guedalia; J. Lee; I. Gonzalez; R. G. Boles
- Book ID
- 111548214
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 186 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0141-8955
No coin nor oath required. For personal study only.