WILLIAM CRAIGEN to F-Box Proteins
This is a "connection" page, showing publications WILLIAM CRAIGEN has written about F-Box Proteins.
Connection Strength
0.240
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FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome. Clin Genet. 2017 Apr; 91(4):634-639.
Score: 0.134
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Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. Am J Hum Genet. 2013 Sep 05; 93(3):471-81.
Score: 0.106