Matches in Nanopublications for { ?s ?p "[Short-chain acyl-CoA dehydrogenase gene variant, with 625 G-to-A and 511 C-to-T changes, impairs C4-C6 fatty acid metabolism and variably causes neonatal/infantile hypotonia with developmental delays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_assertion description "[Short-chain acyl-CoA dehydrogenase gene variant, with 625 G-to-A and 511 C-to-T changes, impairs C4-C6 fatty acid metabolism and variably causes neonatal/infantile hypotonia with developmental delays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.