Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation

✍ Scribed by Eriko Yasaki; Cassandra Prioleau; Julien Barbier; Pascale Richard; Frédéric Andreux; Jean-Paul Leroy; Philippe Dartevelle; Jeanine Koenig; Jordi Molgó; Michel Fardeau; Bruno Eymard; Daniel Hantaı̈

• Book ID: 116792123
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 461 KB
• Volume: 14
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2003.07.002