Citations for
1ACAA1, 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
2ACAA1
Refined localization of human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to 3p22.
Ottone F, et al.
Hum Hered 45 : 75-79. 1995
3RCDP1, 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
4ACAA1
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
Schram AW, et al.
Proc Natl Acad Sci U S A 84 : 2494-2496. 1987