PEX13 Is Mutated in Complementation Group 13 of the Peroxisome-Biogenesis Disorders
✍ Scribed by Yifei Liu; Jonas Björkman; Aaron Urquhart; Ronald J.A. Wanders; Denis I. Crane; Stephen J. Gould
- Book ID
- 117852961
- Publisher
- American Society of Human Genetics
- Year
- 1999
- Tongue
- English
- Weight
- 555 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/302534
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Communicated by Jean-Louis Mandel Peroxisome biogenesis disorders (PBD) are lethal hereditary diseases caused by abnormalities in the biogenesis of peroxisomes. At present, 12 different complementation groups have been identified and to date, all genes responsible for each of these complementat
Diseases of the Zellweger spectrum represent a major subgroup of the peroxisome biogenesis disorders, a group of autosomal-recessive diseases that are characterized by widespread tissue pathology, including neurodegeneration. The Zellweger spectrum represents a clinical continuum, with Zellweger syn