Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: aSacIpolymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis

✍ Scribed by Christina Fuchs; Thomas Liehr; Sevinc Özbey; Arif Ekici; Holger Grehl; B. Rautenstrauss

• Publisher: Springer
• Year: 1998
• Tongue: English
• Weight: 263 KB
• Volume: 2
• Category: Article
• ISSN: 1364-6745
• DOI: 10.1007/s100480050050