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Year | Number of Results |
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1989 | 1 |
1991 | 1 |
1999 | 1 |
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PubMed (OMIM) for id: 30
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Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.
Am J Hum Genet. 2002 Jun;70(6):1589-93. doi: 10.1086/340970. Epub 2002 Apr 23.
Am J Hum Genet. 2002.
PMID: 11992265
Free PMC article.
Characterization of a 1200-kb genomic segment of chromosome 3p22-p21.3.
Daigo Y, Isomura M, Nishiwaki T, Tamari M, Ishikawa S, Kai M, Murata Y, Takeuchi K, Yamane Y, Hayashi R, Minami M, Fujino MA, Hojo Y, Uchiyama I, Takagi T, Nakamura Y.
Daigo Y, et al.
DNA Res. 1999 Feb 26;6(1):37-44. doi: 10.1093/dnares/6.1.37.
DNA Res. 1999.
PMID: 10231028
Free article.
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Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23.
Bout A, Hoovers JM, Bakker E, Mannens MM, Geurts van Kessel A, Westerveld A, Tager JM, Benne R.
Bout A, et al.
Cytogenet Cell Genet. 1989;52(3-4):147-50. doi: 10.1159/000132865.
Cytogenet Cell Genet. 1989.
PMID: 2630187
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Characterization of the gene encoding human peroxisomal 3-oxoacyl-CoA thiolase (ACAA). No large DNA rearrangement in a thiolase-deficient patient.
Bout A, Franse MM, Collins J, Blonden L, Tager JM, Benne R.
Bout A, et al.
Biochim Biophys Acta. 1991 Aug 27;1090(1):43-51. doi: 10.1016/0167-4781(91)90035-k.
Biochim Biophys Acta. 1991.
PMID: 1679347
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