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 |
Externí odkaz: |