Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders

Medicine & Life Sciences

• Complementation Group 7 Peroxisome Biogenesis Disorder 100%
• Peroxisome biogenesis disorders 35%
• Peroxisomes 16%
• Genes 16%
• Proteins 12%
• Mutation 11%
• Yeasts 10%
• Peroxisomal Disorders 10%
• RNA Splice Sites 8%
• Nonsense Codon 7%
• Heterozygote 7%
• Missense Mutation 6%
• Open Reading Frames 6%
• Zinc 6%
• Intellectual Disability 6%
• Exons 5%
• Membrane Proteins 5%
• Fibroblasts 4%
• Alleles 4%
• Phenotype 4%
• Kidney 3%
• Liver 3%