Show
Sort by
-
Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses
-
Episodic positive selection at mitochondrial genome in an introduced biological control agent
-
Mitochondrial function is altered in horse atypical myopathy
-
Clinical, biochemical and genetic spectrum of mitochondrial disorders in Egyptian children : a study of 17 cases
-
Assessment of nuclear transfer techniques to prevent the transmission of heritable mitochondrial disorders without compromising embryonic development competence in mice
-
Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis
-
Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene
-
A new mutation in MT-ND1 m.3928G>C p.V208L causes Leigh disease with infantile spasms
-
Poor correlation between polar bodies and blastomere mutation load in a patient with m.3243A>G tRNALeu(UUR) point mutation
-
Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutation