✦ LIBER ✦

Molecular basis of familial hypercholesterolemia: An Indian experience

✍ Scribed by T. F. Ashavaid; A. K. Altaf; K. G. Nair

Publisher: Association of Clinical Biochemistry of India
Year: 2000
Tongue: English
Weight: 761 KB
Volume: 15
Category: Article
ISSN: 0970-1915
DOI: 10.1007/bf02867540

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The molecular basis of familial hypercho

The molecular basis of familial hypercholesterolemia in The Netherlands

✍ Sigrid W. Fouchier; Joep C. Defesche; Marina A. Umans-Eckenhausen; John J. Kaste 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 97 KB

Update of the molecular basis of familia

Update of the molecular basis of familial hypercholesterolemia in The Netherlands

✍ Sigrid W. Fouchier; John J.P. Kastelein; Joep C. Defesche 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 144 KB 👁 1 views

Autosomal-dominant hypercholesterolemia (ADH) has been identified as a major risk factor for coronary vascular disease (CVD) and is associated with mutations in the low-density lipoprotein receptor (LDLR) and the apolipoprotein B (APOB) gene. Since 1991 DNA samples from clinically diagnosed ADH pati

Molecular genetics of familial hyperchol

Molecular genetics of familial hypercholesterolemia in Israel

✍ Ayeleth Reshef; Henrik Nissen; Liat Triger; Torben Stiig Hensen; Osnat Eliav; Da 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 86 KB

Molecular basis of familial hypercholest

Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations

✍ Luis A. Salazar; Mario H. Hirata; Selma A. Cavalli; Edna R. Nakandakare; Neusa F 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 1 views

## Communicated by Mark H. Paalman Low-density lipoprotein receptor (LDLR) gene mutations cause familial hypercholesterolemia (FH), one of the most common single gene disorders. The spectrum of LDLR mutations in Brazil is not known. The aim of this study was the characterization of LDLR mutations

Identification of two LDL receptor mutat

Identification of two LDL receptor mutations causing familial hypercholesterolemia in Indian subjects

✍ Tester F. Ashavaid; Altaf A. Kondkar; Kappiareth G. Nair 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 161 KB 👁 1 views

Familial hypercholesterolemia (FH) is a genetic disorder caused by numerous mutations in the low-density lipoprotein receptor (LDLR) gene. Mutational analyses of Indians in South Africa suggest the possibility of a high frequency of FH in India. This study aimed at identifying mutations in exons 3,

Molecular characterization of familial h

Molecular characterization of familial hypercholesterolemia in German and Greek patients

✍ George V. Z. Dedoussis; Janine Genschel; Bettina Bochow; Christos Pitsavos; John 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 42 KB 👁 1 views

We used the denaturing gradient gel electrophoresis (DGGE) method to define mutations in the promoter region, the 18 exons, and their flanking intronic sequences of the low-density lipoprotein (LDL) receptor gene LDLR, causing familial hypercholesterolemia (FH) phenotype in 100 German and in 100 Gre