Matches in Nanopublications for { ?s ?p "[Mutations in the TMEM70 gene are the most common cause of nuclear encoded ATP synthase deficiency resulting in a syndrome characterized by neonatal lactic acidosis, cardiomyopathy, and encephalomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_assertion description "[Mutations in the TMEM70 gene are the most common cause of nuclear encoded ATP synthase deficiency resulting in a syndrome characterized by neonatal lactic acidosis, cardiomyopathy, and encephalomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531677.RAXsM8gYl8hRN0IA_AP5gjTP08wTj-b9879wXH66MYKgc130_provenance.
- NP362127.RASdlSZvbtBRqo3IinUT5EOtGcIzgiYbge_sXJUBZMBzw130_assertion description "[Mutations in the TMEM70 gene are the most common cause of nuclear encoded ATP synthase deficiency resulting in a syndrome characterized by neonatal lactic acidosis, cardiomyopathy, and encephalomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362127.RASdlSZvbtBRqo3IinUT5EOtGcIzgiYbge_sXJUBZMBzw130_provenance.
- NP1035660.RAQ_IVxfGRLzIpNzDEbmPFolFJhS4Bg7msvH3eN_pGlnk130_assertion description "[Mutations in the TMEM70 gene are the most common cause of nuclear encoded ATP synthase deficiency resulting in a syndrome characterized by neonatal lactic acidosis, cardiomyopathy, and encephalomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1035660.RAQ_IVxfGRLzIpNzDEbmPFolFJhS4Bg7msvH3eN_pGlnk130_provenance.
- NP915627.RAjakVdkBYTJsAkqaUxDW-iDJrr-we9hRsbNhh-uMMW1Q130_assertion description "[Mutations in the TMEM70 gene are the most common cause of nuclear encoded ATP synthase deficiency resulting in a syndrome characterized by neonatal lactic acidosis, cardiomyopathy, and encephalomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915627.RAjakVdkBYTJsAkqaUxDW-iDJrr-we9hRsbNhh-uMMW1Q130_provenance.