Two novel CLN5 mutations in a Portuguese patient with vLINCL: Insights into molecular mechanisms of CLN5 deficiency

✍ Scribed by C. Bessa; C.A.F. Teixeira; M. Mangas; A. Dias; M.C. Sá Miranda; A. Guimarães; J.C. Ferreira; N. Canas; P. Cabral; M.G. Ribeiro

• Book ID: 116987864
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 825 KB
• Volume: 89
• Category: Article
• ISSN: 1096-7192
• DOI: 10.1016/j.ymgme.2006.04.010