Pages that link to "Q74570537"
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The following pages link to Possible role of mtDNA mutations in sudden infant death (Q74570537):
Displaying 10 items.
- The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family (Q35065160) (← links)
- Sudden unexpected death and covert homicide in infancy (Q35279361) (← links)
- Heterogeneous natural selection on oxidative phosphorylation genes among fishes with extreme high and low aerobic performance (Q35755091) (← links)
- Mitochondrial DNA as a cancer biomarker (Q35789945) (← links)
- Gene variants predisposing to SIDS: current knowledge (Q37771900) (← links)
- Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course (Q37970121) (← links)
- Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic. (Q44996544) (← links)
- Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS. (Q47401355) (← links)
- Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC). (Q50094252) (← links)
- Mutations in mitochondrial DNA associated with hypertension (Q84998195) (← links)