Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene

✍ Scribed by Tanya Stojkovic; Philippe Latour; Ghislaine Viet; Jérôme de Seze; Jean-François Hurtevent; Antoon Vandenberghe; P. Vermersch

• Book ID: 116792159
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 120 KB
• Volume: 14
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2004.01.003