Matches in Nanopublications for { ?s ?p "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_assertion description "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- NP386055.RA_xqCjP2FcbZ-IunQa6hRphBC8rjVsW4i6cV7SqNHCqk130_assertion description "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386055.RA_xqCjP2FcbZ-IunQa6hRphBC8rjVsW4i6cV7SqNHCqk130_provenance.
- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion description "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_provenance.