| 1 | ACAA1, EHHADH, PBE |
| Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein. | |
| Ferdinandusse S, van Grunsven EG, Oostheim W, Denis S, Hogenhout EM, IJlst L, van Roermund CW, Waterham HR, Goldfischer S, Wanders RJ. | |
| Am J Hum Genet 70(6):1589-93. Epub 2002 Apr 23. 2002 | |
| 2 | ACAA1 |
| Refined localization of human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to 3p22. | |
| Ottone F, et al. | |
| Hum Hered 45 : 75-79. 1995 | |
| 3 | RCDP1, ACAA1 |
| Characterization of the gene encoding human peroxisomal 3-oxoacyl-CoA thiolase (ACAA). No large DNA rearrangement in a thiolase-deficient patient. | |
| Bout A, et al. | |
| Biochim Biophys Acta 1090(1):43-51 1991 | |
| 4 | ACAA1 |
| Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency. | |
| Schram AW, et al. | |
| Proc Natl Acad Sci U S A 84 : 2494-2496. 1987 | |