Links
[1] http://www.ncbi.nlm.nih.gov/omim/302950
[2] http://www.ncbi.nlm.nih.gov/omim/118651
[3] http://ghr.nlm.nih.gov/gene/PEX7
[4] https://disorders.eyes.arizona.edu/disorders/peroxisome-biogenesis-disorder-1a-zellweger
[5] http://www.ncbi.nlm.nih.gov/omim/214100
[6] https://disorders.eyes.arizona.edu/disorders/peroxisome-biogenesis-disorder-3b-infantile-refsum-disease
[7] http://www.ncbi.nlm.nih.gov/omim/266510
[8] https://disorders.eyes.arizona.edu/disorders/refsum-disease-adult
[9] http://www.ncbi.nlm.nih.gov/omim/266500
[10] https://disorders.eyes.arizona.edu/references/mutational-spectrum-pex7-gene-and-functional-analysis-mutant-alleles-78-patients-0
[11] https://disorders.eyes.arizona.edu/references/cataracts-marker-genetic-heterogeneity-chondrodysplasia-punctata-0