Matches in Nanopublications for { ?s ?p "[Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused by mutations in two genes, KCNQ2 and KCNQ3, encoding for potassium channel subunits underlying the M-current.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP359887.RAj9xdizf8NRjp6FPnmtuZXTH6kruOvmzX5kNN9R1bbZg130_assertion description "[Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused by mutations in two genes, KCNQ2 and KCNQ3, encoding for potassium channel subunits underlying the M-current.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359887.RAj9xdizf8NRjp6FPnmtuZXTH6kruOvmzX5kNN9R1bbZg130_provenance.
- NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_assertion description "[Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused by mutations in two genes, KCNQ2 and KCNQ3, encoding for potassium channel subunits underlying the M-current.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841681.RAqF0WREoACanCgaVHeNHPqQ16bf65INy0MzTJwXTvgJo130_provenance.