Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.: An article from: Human Biology

This digital document is an article from Human Biology, published by Thomson Gale on October 1, 2005. The length of the article is 4221 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the author: KEY WORDS: FAMILIAL DEFECTIVE APOB, AUTOSOMAL DOMINANT MONOGENIC HYPERCHOLESTEROLEMIA (ADMH), HYPERCHOLESTEROLEMIA, APOB, LDLR, R3500Q MUTATION, T3552T MUTATION, SSCP (SINGLE-STRAND CONFORMATION POLYMORPHISM) ANALYSIS, SPAIN.

Citation Details
Title: Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.
Author: Erardo Merino-Ibarra
Publication:Human Biology (Magazine/Journal)
Date: October 1, 2005
Publisher: Thomson Gale
Volume: 77 Issue: 5 Page: 663(11)

Distributed by Thomson Gale