186 NOVEL ABCA1 MUTATIONS IN L PATIENTS WITH SEVERE HDL DEFICIENCY WITH OR WITHOUT CLASSIC MANIFESTATIONS OF TANGIER DISEASE

✍ Scribed by Zanoni, P.; Fasano, T.; Deegan, P.B.; Park, A.; Feher, M.D.; Gurakan, F.; Favari, E.; Bernini, F.; Calandra, S.

• Book ID: 118639193
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 41 KB
• Volume: 12
• Category: Article
• ISSN: 1567-5688
• DOI: 10.1016/s1567-5688(11)70187-8