PEX13 Is Mutated in Complementation Group 13 of the Peroxisome-Biogenesis Disorders
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference57 articles.
1. Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways;Albertini;Cell,1997
2. cDNA sequence coding for human kidney catalase;Bell;Nucleic Acids Res,1986
3. Genomic structure of PEX13: a candidate peroxisome biogenesis disorder gene;Bjorkman;Genomics,1998
4. Sequence of a putative human housekeeping gene (HK33) localized on chromosome 1;Braun;Gene,1994
5. Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata;Braverman;Nat Genet,1997
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