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3. Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients. Maxwell MA; Allen T; Solly PB; Svingen T; Paton BC; Crane DI Hum Mutat; 2002 Nov; 20(5):342-51. PubMed ID: 12402331 [TBL] [Abstract][Full Text] [Related]
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10. Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders. Reuber BE; Germain-Lee E; Collins CS; Morrell JC; Ameritunga R; Moser HW; Valle D; Gould SJ Nat Genet; 1997 Dec; 17(4):445-8. PubMed ID: 9398847 [TBL] [Abstract][Full Text] [Related]
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