Identification of PEX10, the Gene Defective in Complementation Group 7 of the Peroxisome-Biogenesis Disorders
Open Access
- 1 August 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (2) , 347-359
- https://doi.org/10.1086/301963
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Identification of PAHX, a Refsum disease geneNature Genetics, 1997
- A unified nomenclature for peroxisome biogenesis factors.The Journal of cell biology, 1996
- Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor.The Journal of cell biology, 1996
- Analysis of the Carboxyl-terminal Peroxisomal Targeting Signal 1 in a Homologous Context in Saccharomyces cerevisiaeJournal of Biological Chemistry, 1996
- The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop.The Journal of cell biology, 1996
- Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groupsThe Journal of Pediatrics, 1995
- The Hansenula polymorpha PER3 Gene Is Essential for the Import of PTS1 Proteins into the Peroxisomal MatrixPublished by Elsevier ,1995
- The Hansenula polymorpha PER8 gene encodes a novel peroxisomal integral membrane protein involved in proliferation.The Journal of cell biology, 1995
- BIOCHEMISTRY OF PEROXISOMESAnnual Review of Biochemistry, 1992
- Strand-separating conformational polymorphism analysis: Efficacy of detection of point mutations in the human ornithine δ-aminotransferase geneGenomics, 1992