Links
[1] http://ghr.nlm.nih.gov/search?query=Pex&Search=
[2] http://ghr.nlm.nih.gov/gene/PEX1
[3] http://ghr.nlm.nih.gov/gene/PEX2
[4] http://ghr.nlm.nih.gov/gene/PEX3
[5] http://ghr.nlm.nih.gov/gene/PEX12
[6] http://ghr.nlm.nih.gov/gene/PEX26
[7] https://disorders.eyes.arizona.edu/disorders/peroxisome-biogenesis-disorder-1a-zellweger
[8] http://omim.org/entry/214100
[9] https://disorders.eyes.arizona.edu/disorders/rhizomelic-chondrodysplasia-punctata
[10] http://omim.org/entry/215100
[11] https://disorders.eyes.arizona.edu/disorders/peroxisome-biogenesis-disorder-1b-neonatal-adrenoleukodystrophy
[12] http://omim.org/entry/601539
[13] https://disorders.eyes.arizona.edu/references/newly-identified-milder-phenotype-peroxisome-biogenesis-disorder-caused-mutated-pex3-gene
[14] https://disorders.eyes.arizona.edu/references/genetics-and-molecular-basis-human-peroxisome-biogenesis-disorders
[15] https://disorders.eyes.arizona.edu/references/infantile-refsum-disease-neonatal-cholestatic-jaundice-presentation-peroxisomal-disorder
[16] https://disorders.eyes.arizona.edu/references/genetic-relation-between-zellweger-syndrome-infantile-refsums-disease-and-rhizomelic