Ceyhan-Birsoy, O., Talim, B., Swanson, L. C., Karakaya, M., Graff, M. A., Beggs, A. H., & Topaloglu, H. (2015). Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement. J Neuromuscul Dis.
Stile di citazione ChicagoCeyhan-Birsoy, Ozge, Beril Talim, Lindsay C. Swanson, Mert Karakaya, Michelle A. Graff, Alan H. Beggs, e Haluk Topaloglu. "Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement." J Neuromuscul Dis 2015.
Citazione MLACeyhan-Birsoy, Ozge, et al. "Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement." J Neuromuscul Dis 2015.