𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria

✍ Scribed by Bernard Grandchamp; Jerome Lamoril; Hervé Puy


Book ID
105465532
Publisher
Springer US
Year
1995
Tongue
English
Weight
387 KB
Volume
27
Category
Article
ISSN
0145-479X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Systematic analysis of coproporphyrinoge
✍ R. Rosipal; J. Lamoril; H. Puy; V. Da Silva; L. Gouya; F.W.M. De Rooij; K. Te Ve 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 478 KB 👁 2 views

## Communicated by Peter Byers Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (CPO). Clinical manifestations of the disease are characterized by acute attacks of neurological dysfunctio