Identification of a homozygous pex26 mutation in a heimler syndrome patient

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• Sample 40%
• Phenotype 40%
• Chromosome 40%
• Temperature Sensitivity 40%
• Exome Sequencing 40%
• Nested Gene 20%
• DNA 20%
• Comprehension 20%
• Sequencing 20%
• Mutant 20%
• Hearing 20%
• Catalase 20%
• Proband 20%
• Amelogenesis 20%
• Bioinformatics 20%
• Molecular Genetics 20%