Metabolism as a complex genetic trait, a systems biology approach: Implications for inborn errors of metabolism and clinical diseases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-008-1005-8
Reference64 articles.
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3. Bennett MJ, Weinberger MJ, Sherwood WG, Burlina AB (1994) Secondary 3-hydroxydicarboxylic aciduria mimicking long chain 3-hydroxyacyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 17: 283–286. doi: 10.1007/BF00711808 .
4. Bennett MJ, Rinaldo P, Strauss AW (2000) Inborn errors of mitochondrial fatty acid oxidation. Crit Rev Clin Lab Sci 37: 1–44. doi: 10.1080/10408360091174169 .
5. Brand MD, D’Alessandri L, Reis HM, Hafner RP (1990). Stimulation of the electron transport chain in mitochondria isolated from rats treated with mannoheptulose or glucagon. Arch Biochem Biophys 283: 278–284. doi: 10.1016/0003-9861(90)90643-D .
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