Preferred Label : apolipoprotein C-II (Toronto);
MeSH note : a nonfunctional human mutant apoC-II identified in Toronto; involves a nucleotide
deletion in the codon for either Thr68 or Asp69 and a translation reading frame shift;
caused apoC-II deficiency;
MeSH synonym : apolipoprotein C-II, Toronto; apo C-II, Toronto; apoC-II (Toronto); apolipoprotein C-IIToronto;
Registry Number MeSH : 107497-50-7;
Is substance : O;
Origin ID : C050929;
UMLS CUI : C0245042;
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