Author:
Walter Claudia,Gootjes Jeannette,Mooijer Petra A.,Portsteffen Herma,Klein Christina,Waterham Hans R.,Barth Peter G.,Epplen Jörg T.,Kunau Wolf-H.,Wanders Ronald J.A.,Dodt Gabriele
Subject
Genetics(clinical),Genetics
Reference39 articles.
1. Protein misfolding and degradation in genetic diseases;Bross;Hum Mutat,1999
2. Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children;Budden;J Pediatr,1986
3. Identification of a common PEX1 mutation in Zellweger syndrome;Collins;Hum Mutat,1999
4. The peroxisome biogenesis factors pex4p, pex22p, pex1p, and pex6p act in the terminal steps of peroxisomal matrix protein import;Collins;Mol Cell Biol,2000
5. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders;Dodt;Nat Genet,1995
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