Key result
Novel APOB mutations cause apolipoprotein B truncations that are undetectable in plasma and result in familial hypobetalipoproteinemia.
This is an erratum correcting a specific point mutation location in a previously published article.
Erratum corrects APOB mutation annotation; leaves open functional validation of these variants in hypobetalipoproteinemia.
The following error was found in the original version of this article: In Family 98, a novel point mutation in exon 26 (11163T4G) referring to GenBank number XM_036735 should be 11168T4G.
No takes yet. Share an insight, caveat, or question.
Yue et al. (2002) studied this question. Novel APOB mutations cause apolipoprotein B truncations that are undetectable in plasma and result in familial hypobetalipoproteinemia.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: