Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype
Author:
Affiliation:
1. ; Department of Paediatrics; Heinrich Heine University Düsseldorf; Moorenstrasse 5 Düsseldorf D-40225 Germany
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005599903632/fullpdf
Reference8 articles.
1. The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop;Dyer;J Cell Biol,1996
2. Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome;Gärtner;Nature Genetics,1992
3. A conserved tripeptide sorts proteins to peroxisomes;Gould;J Cell Biol,1989
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