W14.347 Mutations in LCAT gene causing familial LCAT deficiency, fish eye disease and co-dominant familial HDL deficiency

✍ Scribed by Bertolini, S.; Calabresi, L.; Pisciotta, L.; Balboni, M.; Arca, M.; Cantafora, A.; Franceshini, G.; Calandra, S.

• Book ID: 118632741
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 147 KB
• Volume: 5
• Category: Article
• ISSN: 1567-5688
• DOI: 10.1016/s1567-5688(04)90346-2