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1988 | 1 |
1993 | 1 |
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Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.
Am J Hum Genet. 1993 Apr;52(4):843-4.
Am J Hum Genet. 1993.
PMID: 7681622
Free PMC article.
No abstract available.
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM.
Brul S, et al.
J Clin Invest. 1988 Jun;81(6):1710-5. doi: 10.1172/JCI113510.
J Clin Invest. 1988.
PMID: 2454948
Free PMC article.
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