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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1981 1
1985 1
1987 1
1988 2
1989 1
1992 3
1993 1
1995 1
1996 1
1997 2
1998 1
2000 1
2001 2
2002 2
2003 2
2024 0

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PubMed (OMIM) for id: 316820

23 results

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Page 1
Organization of the human liver carnitine palmitoyltransferase 1 gene ( CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia.
Gobin S, Bonnefont JP, Prip-Buus C, Mugnier C, Ferrec M, Demaugre F, Saudubray JM, Rostane H, Djouadi F, Wilcox W, Cederbaum S, Haas R, Nyhan WL, Green A, Gray G, Girard J, Thuillier L. Gobin S, et al. Hum Genet. 2002 Aug;111(2):179-89. doi: 10.1007/s00439-002-0752-0. Epub 2002 Jul 16. Hum Genet. 2002. PMID: 12189492
Features of carnitine palmitoyltransferase type I deficiency.
Olpin SE, Allen J, Bonham JR, Clark S, Clayton PT, Calvin J, Downing M, Ives K, Jones S, Manning NJ, Pollitt RJ, Standing SJ, Tanner MS. Olpin SE, et al. J Inherit Metab Dis. 2001 Feb;24(1):35-42. doi: 10.1023/a:1005694320063. J Inherit Metab Dis. 2001. PMID: 11286380
23 results