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fbxl4
- FBXL4-related encephalomyopathic mitochondrial DNA (mtDNA) depletion syndrome is a severe condition that begins in infancy and ... dysfunction combined with muscle weakness (encephalomyopathy).Infants with FBXL4-related encephalomyopathic mtDNA depletion syndrome have weak muscle ...
- The FBXL4 gene provides instructions for making a member of a family of proteins called F-box and leucine rich repeat proteins. Like other members of this ...
- Mitochondrial Diseases (National Library of Medicine)Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
- ... Leigh syndrome. BCS1L BTD DLAT DLD EARS2 ETHE1 FBXL4 GFM1 MT-ATP6 MT-ND1 MT-ND4 MT- ...