Matches in Nanopublications for { ?s ?p "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1475.RAgZH9kV7y9iix4B2uH65Srjz1LyoJw6B9TOxVlVmVQ10130_provenance.
- assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_provenance.
- NP323388.RAZVUWHXQPSCktb4lNqpN16EWQsH6iHBHb4G3LZecQ5A0130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323388.RAZVUWHXQPSCktb4lNqpN16EWQsH6iHBHb4G3LZecQ5A0130_provenance.
- NP3409.RA68bCaluLj1Vh8yqM7GI0tNNmizuAU2UHAXBtKSq1hYU130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3409.RA68bCaluLj1Vh8yqM7GI0tNNmizuAU2UHAXBtKSq1hYU130_provenance.
- NP2833.RAA1IrXVFGNwTEUbVuaflST8TEuZeRbXVzMnDNNItyUgQ130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2833.RAA1IrXVFGNwTEUbVuaflST8TEuZeRbXVzMnDNNItyUgQ130_provenance.
- NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406132.RAFjkjuGZr8cmVROvBG90n-qzkkQlSH-PCi2c7Na4NuOE130_provenance.