Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies

✍ Scribed by Ian J Sutton; A Paul Mocroft; Victoria H Lindley; Richard M Barber; R Jane Bryon; John B Winer; Fiona MacDonald

• Book ID: 116792231
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 197 KB
• Volume: 14
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2004.07.006