1. van den Brink, Daan M, Brites, Pedro, Haasjes, Janet, Waterham, Hans R, Wanders, Ronald J A. 2003. Identification of PEX7 as the second gene involved in Refsum disease. In American journal of human genetics, 72, 471-7. doi:. https://pubmed.ncbi.nlm.nih.gov/12522768/
2. Steinberg, Steven J, Dodt, Gabriele, Raymond, Gerald V, Moser, Ann B, Moser, Hugo W. 2006. Peroxisome biogenesis disorders. In Biochimica et biophysica acta, 1763, 1733-48. doi:. https://pubmed.ncbi.nlm.nih.gov/17055079/
3. Braverman, N, Steel, G, Lin, P, Moser, H, Valle, D. . PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter. In Genomics, 63, 181-92. doi:. https://pubmed.ncbi.nlm.nih.gov/10673331/
4. Fallatah, Wedad, Cui, Wei, Di Pietro, Erminia, Berger, Johannes, Braverman, Nancy E. 2022. A Pex7 Deficient Mouse Series Correlates Biochemical and Neurobehavioral Markers to Genotype Severity-Implications for the Disease Spectrum of Rhizomelic Chondrodysplasia Punctata Type 1. In Frontiers in cell and developmental biology, 10, 886316. doi:10.3389/fcell.2022.886316. https://pubmed.ncbi.nlm.nih.gov/35898397/
5. Shin, Jong-Hwan, Fu, Teng, Kim, Kyoung Su. 2021. Pex7 selectively imports PTS2 target proteins to peroxisomes and is required for anthracnose disease development in Colletotrichum scovillei. In Fungal genetics and biology : FG & B, 157, 103636. doi:10.1016/j.fgb.2021.103636. https://pubmed.ncbi.nlm.nih.gov/34742890/
6. Pridie, C, Simmonds, Andrew J. 2020. The role of Peroxin 7 during Drosophila embryonic development. In Genome, 64, 119-137. doi:10.1139/gen-2019-0207. https://pubmed.ncbi.nlm.nih.gov/32191843/
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