Publication | Open Access

Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation

Complement SystemAllelic VariantDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsPathogenesisMolecular GeneticsDisease Gene IdentificationGene ExpressionMedicineRedox BiologyComplementation Group 8Cause Peroxisome-biogenesis DisordersGenotype-phenotype Correlation