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cpt1a in Homo sapiensMus musculusRattus norvegicusAll 437 Gene records
GeneReviews® [Internet].
Adam MP, Feldman J, Mirzaa GM, et al., editors.
Seattle (WA): University of Washington, Seattle; 1993-2024.
GeneReviews by Title GeneReviews Advanced Search Help
Carnitine Palmitoyltransferase 1A Deficiency.
Bennett MJ, Santani AB. 2005 Jul 27 [Updated 2016 Mar 17].
Multiple Acyl-CoA Dehydrogenase Deficiency.
Prasun P. 2020 Jun 18.
Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in the Hutterite Population.
Wallace SE, Bean LJH. 2020 May 7 [Updated 2022 Dec 1].
Long-Chain Hydroxyacyl-CoA Dehydrogenase Deficiency / Trifunctional Protein Deficiency.
Prasun P, LoPiccolo MK, Ginevic I. 2022 Sep 1.
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency.
Merritt JL 2nd, Chang IJ. 2000 Apr 20 [Updated 2019 Jun 27].
Carnitine Palmitoyltransferase II Deficiency.
Wieser T. 2004 Aug 27 [Updated 2019 Jan 3].
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