| 1 | PEX14, PBD10
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| Identification of a novel PEX14 mutation in Zellweger syndrome.
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| Huybrechts SJ, Van Veldhoven PP, Hoffman I, Zeevaert R, de Vos R, Demaerel P, Brams M, Jaeken J, Fransen M, Cassiman D.
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| J Med Genet 45(6):376-383. Epub 2008 Feb 19. 2008
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| 2 | PBD1, PBD2, PBD3, PBD4, PBD5, PBD6, PBD7, PBD8, PBD9, PBD10
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| Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders.
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| Wanders RJ, Waterham HR.
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| Clin Genet 67(2):107-33. Review. 2005
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| 3 | PEX14, PBD10
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| Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
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| Shimotawa N, Tsukamoto T, Nagase T, Takemoto Y, Koyama N, Suzuki Y, Komori M, Osumi T, Jeannette G, Wanders RJ, Kondo N.
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| Hum Mutat 23(6):552-8. 2004
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| 4 | PBD1, PBD2, PBD3, PBD4, PBD5, PBD6, PBD8, PBD9, PBD10
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| Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patients.
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| Poll-The BT, Gootjes J, Duran M, De Klerk JB, Wenniger-Prick LJ, Admiraal RJ, Waterham HR, Wanders RJ, Barth PG.
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| Am J Med Genet A 126(4):333-8. 2004
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