Matches in Nanopublications for { ?s ?p "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_provenance.
- NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70096.RAys85RE0sfX-cxmATYcFpIP09DfyO-WFNXJLX17lx9Q0130_provenance.
- NP76497.RAqdfI8HZ-1SAY2dCtTka9LPq9bglz9y_IaYIuwQcRqQA130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76497.RAqdfI8HZ-1SAY2dCtTka9LPq9bglz9y_IaYIuwQcRqQA130_provenance.
- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_provenance.