A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany

✍ Scribed by Carsten Bergmann; J.Michael Schröder; Sabine Rudnik-Schöneborn; Klaus Zerres; Jan Senderek

• Book ID: 117385641
• Publisher: Elsevier Science
• Year: 2001
• Tongue: English
• Weight: 41 KB
• Volume: 88
• Category: Article
• ISSN: 0169-328X
• DOI: 10.1016/s0169-328x(01)00040-7