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The molecular basis of human complex I deficiency.
Tucker EJ, Compton AG, Calvo SE, Thorburn DR. Tucker EJ, et al. IUBMB Life. 2011 Sep;63(9):669-77. doi: 10.1002/iub.495. Epub 2011 Jul 15. IUBMB Life. 2011. PMID: 21766414 Free article. Review.
Disorders of oxidative phosphorylation (OXPHOS) have a birth prevalence of 1/5,000 and are the most common inborn errors of metabolism. The most common OXPHOS disorder is complex I deficiency. ...Molecular diagnosis of patients with complex I defici
Disorders of oxidative phosphorylation (OXPHOS) have a birth prevalence of 1/5,000 and are the most common inborn errors of metabolis …
Genetics of type 2 diabetes mellitus.
Malecki MT. Malecki MT. Diabetes Res Clin Pract. 2005 Jun;68 Suppl1:S10-21. doi: 10.1016/j.diabres.2005.03.003. Epub 2005 Mar 19. Diabetes Res Clin Pract. 2005. PMID: 15955369 Review.
The clinical picture of type 2 diabetes mellitus (T2DM) is formed by impairment in insulin secretion and resistance to insulin action. ...The majority of proteins associated with MODY are transcription factors, such as hepatocyte nuclear factor 4alpha (HNF-4alpha), …
The clinical picture of type 2 diabetes mellitus (T2DM) is formed by impairment in insulin secretion and resistance to insulin action …