𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Structure of the PCCA Gene and Distribution of Mutations Causing Propionic Acidemia

✍ Scribed by Eric Campeau; Lourdes R. Desviat; Daniel Leclerc; Xuchu Wu; Belén Pérez; Magdalena Ugarte; Roy A. Gravel


Book ID
115639885
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
215 KB
Volume
74
Category
Article
ISSN
1096-7192

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Overview of mutations in the PCCA and PC
✍ Magdalena Ugarte; Celia Pérez-Cerdá; Pilar Rodríguez-Pombo; Lourdes R. Desviat; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 296 KB 👁 2 views

Propionic acidemia is an inborn error of metabolism caused by a deficiency of propionyl-CoA carboxylase, a heteropolymeric mitochondrial enzyme involved in the catabolism of branched chain amino acids, odd-numbered chain length fatty acids, cholesterol, and other metabolites. The enzyme is composed