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Article

Detection of a novel mutation (stop 468) in exon 10 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians.

Human molecular genetics - 1 Sept 1994

Simard J, Moorjani S, Vohl M C, Couture P, Torres A L, Gagné C, Després J P, Labrie F, Lupien P J

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 7833932
DOI: 10.1093/hmg/3.9.1689

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Detection of a novel mutation (stop 468) in exon 10 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians.PMID 7833932Read ↗

Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians.Semantic proximity Read ↗

A novel V415A mutation in exon 9 of the low density lipoprotein receptor gene causing familial hypercholesterolemia.Semantic proximity Read ↗

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Identification of three new mutations of the low density lipoprotein receptor gene in Dutch familial hypercholesterolemic patients.Semantic proximity Read ↗

A novel mutation M-21V in exon 1 of the low density lipoprotein receptor gene causing familial hypercholesterolemia.Semantic proximity Read ↗

Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemia.Semantic proximity Read ↗

Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemia.Semantic proximity Read ↗

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