✦ LIBER ✦

Familial defective apolipoprotein B-100: a mutation emerged in the Mesolithic ancestors of Celtic peoples?

✍ Scribed by André R Miserez; Patrick Y Muller

Book ID: 119438764
Publisher: Elsevier Science
Year: 2000
Tongue: English
Weight: 280 KB
Volume: 148
Category: Article
ISSN: 0021-9150
DOI: 10.1016/s0021-9150(99)00470-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Familial defective apolipoprotein B-100:

Familial defective apolipoprotein B-100: a mutation emerged in the Mesolithic period

✍ A.R. Miserez; P.Y. Muller 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 56 KB

Familial defective apolipoprotein B-100

Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele

✍ Laila O Abdel-Wareth; Simon N Pimstone; Jean-Pierre Lagarde; Alain Raisonnier; P 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 128 KB

Familial defective apolipoprotein B-100

Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene

✍ Bednarska-Makaruk, Małgorzata; Bisko, Mariola; Puławska, Maria F; Hoffman-Zachar 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 197 KB

Familial defective apolipoprotein B-100:

Familial defective apolipoprotein B-100: detection and haplotype analysis of the Arg3500→Gln mutation in hyperlipidemic Chinese

✍ Yen-Ni Teng; Ju-Pin Pan; Shiu-Ching Chou; Der-Yan Tai; Guey-Jen Lee-Chen 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 129 KB

Familial ligand-defective apolipoprotein

Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK

✍ Philip R Wenham; Bryony G Henderson; Michael D Penney; J.Peter Ashby; Peter W.H 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 349 KB

Familial ligand-defective apolipoprotein

Familial ligand-defective apolipoprotein B-100: Simultaneous detection of the ARG3500→GLN and ARG3531→CYS mutations in a French population

✍ JP Rabès; M Varret; B Saint-Jore; D Erlich; G Jondeau; M Krempf; P Giraudet; C J 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 161 KB

## Communicated by Michel Goossens Familial ligand-defective apolipoprotein B-100 (FDB) is an autosomal dominant disorder leading to plasma LDL cholesterol elevation and coronary artery disease (CAD). Two specific mutations in the APOB gene-R3500Q and R3531C-induce FDB. We report an original metho