Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation
Eriko Yasaki, Cassandra Prioleau, Julien Barbier, Pascale Richard, Frédéric Andreux, Jean-Paul Leroy, Philippe Dartevelle, Jeanine Koenig, Jordi Molgó, Michel Fardeau, Bruno Eymard, Daniel Hantaı̈Volume:
14
Year:
2004
Language:
english
DOI:
10.1016/j.nmd.2003.07.002
File:
PDF, 461 KB
english, 2004