Publication | Closed Access
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
569
Citations
26
References
1999
Year
CardiomyopathyHeart FailureGenetic DisorderGeneticsPathologyCongenital Heart DefectCongenital Heart AnomalyCox Assembly GeneMedicineCardiologyFatal Infantile CardioencephalomyopathyCardiovascular GeneticsCox Deficiency
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