Screening for mutations in charcotmarie-tooth type 1A (CMT1A) disease and hereditary neuropathy with liability to pressure palsies (HNPP)

✍ Scribed by A. Löfgren; V. Timmerman; E. Nelis; P. de Jonghe; J.-J. Martin; C. Van Broeckhoven

• Book ID: 116168864
• Publisher: Elsevier Science
• Year: 1996
• Tongue: English
• Weight: 113 KB
• Volume: 6
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/0960-8966(96)89012-2