Autosomal dominant nemaline myopathy: A new phenotype unlinked to previously known genetic loci

Autor: Jeannet, P.Y., Mittaz, L., Dunand, M., Lobrinus, J.A., Bonafe, L., Kuntzer, T.
Zdroj: In Neuromuscular Disorders 2007 17(1):6-12
Databáze: ScienceDirect