Vyzkoušejte nový nástroj s podporou AI
Summon Research Assistant
BETA
Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2
Mitsuhashi, Satomi, Boyden, Steven E., Estrella, Elicia A., Jones, Takako I., Rahimov, Fedik, Yu, Timothy W., Darras, Basil T., Amato, Anthony A., Folkerth, Rebecca D., Jones, Peter L., Kunkel, Louis M., Kang, Peter B.
Published in Neuromuscular disorders : NMD (01.12.2013)
Published in Neuromuscular disorders : NMD (01.12.2013)
Get full text
Journal Article