A novel LCAT mutation (Phe382→Val) in a kindred with familial LCAT deficiency and defective apolipoprotein B-100

✍ Scribed by M.Nazeem Nanjee; Joseph Stocks; C.Justin Cooke; Henri O.F Molhuizen; Santica Marcovina; David Crook; John P Kastelein; Norman E Miller

• Book ID: 119435928
• Publisher: Elsevier Science
• Year: 2003
• Tongue: English
• Weight: 259 KB
• Volume: 170
• Category: Article
• ISSN: 0021-9150
• DOI: 10.1016/s0021-9150(03)00241-7