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- NP645513.RAJmL6G2DmNjL6BN3D8VukNJbfYbmcw6l2V29DNCWJHNw130_assertion type Assertion NP645513.RAJmL6G2DmNjL6BN3D8VukNJbfYbmcw6l2V29DNCWJHNw130_head.
- NP645513.RAJmL6G2DmNjL6BN3D8VukNJbfYbmcw6l2V29DNCWJHNw130_assertion description "[These data indicate that mutations in SCO2 cause a fatal infantile mitochondrial disorder characterized by hypertrophic cardiomyopathy and encephalopathy, and point to the presence of one or more other genes, perhaps in the copper delivery pathway, in this clinical phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645513.RAJmL6G2DmNjL6BN3D8VukNJbfYbmcw6l2V29DNCWJHNw130_provenance.
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