Genetic defects causing familial hypercholesterolaemia: Identification of deletions and duplications in the LDL-receptor gene and summary of all mutations found in patients attending the Hammersmith Hospital Lipid Clinic

✍ Scribed by Isabella Tosi; Paola Toledo-Leiva; Clare Neuwirth; Rossi P. Naoumova; Anne K. Soutar

• Book ID: 118421451
• Publisher: Elsevier Science
• Year: 2007
• Tongue: English
• Weight: 643 KB
• Volume: 194
• Category: Article
• ISSN: 0021-9150
• DOI: 10.1016/j.atherosclerosis.2006.10.003