Matches in Nanopublications for { ?s ?p "[Mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria is associated with mutations in SUCLA2, the gene encoding a beta subunit of succinate-CoA ligase, where 17 patients have been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP212566.RAbxgSfVqSXxwPKbmOcTXXz-xLRvcc9gU1M5FOGDF76Ak130_assertion description "[Mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria is associated with mutations in SUCLA2, the gene encoding a beta subunit of succinate-CoA ligase, where 17 patients have been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212566.RAbxgSfVqSXxwPKbmOcTXXz-xLRvcc9gU1M5FOGDF76Ak130_provenance.
- NP167110.RApLgtFRPQGOA5pdjYqJ6kDn2t4zNrtFlFE3MsRD8SuH8130_assertion description "[Mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria is associated with mutations in SUCLA2, the gene encoding a beta subunit of succinate-CoA ligase, where 17 patients have been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167110.RApLgtFRPQGOA5pdjYqJ6kDn2t4zNrtFlFE3MsRD8SuH8130_provenance.