Chú thích ACADM

  1. ↑ “Human PubMed Reference:”.
  2. ↑ ]Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (tháng 10 năm 2013). “Integration of cardiac proteome biology and medicine by a specialized knowledgebase”. Circulation Research. 113 (9): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
  3. ↑ “Mitochondrially encoded NADH dehydrogenase 1”. Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Bản gốc lưu trữ ngày 24 tháng 9 năm 2015. Truy cập ngày 7 tháng 6 năm 2018.
  4. ↑ Matsubara Y, Kraus JP, Yang-Feng TL, Francke U, Rosenberg LE, Tanaka K (tháng 9 năm 1986). “Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1”. Proceedings of the National Academy of Sciences of the United States of America. 83 (17): 6543–7. doi:10.1073/pnas.83.17.6543. PMC 386540. PMID 3462713.
  5. ↑ Goetzman ES, Alcorn JF, Bharathi SS, Uppala R, McHugh KJ, Kosmider B, Chen R, Zuo YY, Beck ME, McKinney RW, Skilling H, Suhrie KR, Karunanidhi A, Yeasted R, Otsubo C, Ellis B, Tyurina YY, Kagan VE, Mallampalli RK, Vockley J (tháng 4 năm 2014). “Long-chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction”. The Journal of Biological Chemistry. 289 (15): 10668–79. doi:10.1074/jbc.M113.540260. PMC 4036448. PMID 24591516.
  6. ↑ Pagon RA, Bird TD, Dolan CR, và đồng nghiệp (1993). “Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency”. PMID 20301597. Chú thích journal cần |journal= (trợ giúp)
  7. ↑ Gregersen N, Andresen BS, Bross P, Winter V, Rüdiger N, Engst S, Christensen E, Kelly D, Strauss AW, Kølvraa S (tháng 4 năm 1991). “Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli”. Human Genetics. 86 (6): 545–51. doi:10.1007/bf00201539. PMID 1902818.
  8. ↑ Sturm M, Herebian D, Mueller M, Laryea MD, Spiekerkoetter U (2012). “Functional effects of different medium-chain acyl-CoA dehydrogenase genotypes and identification of asymptomatic variants”. PLOS ONE. 7 (9): e45110. doi:10.1371/journal.pone.0045110. PMC 3444485. PMID 23028790.

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