Congenital Muscular Dystrophy
Publisher
Springer New York
Reference46 articles.
1. Aida, N. (1998). Fukuyama congenital muscular dystrophy: A neuroradiologic review. Journal of Magnetic Resonance Imaging, 8, 317–326. 2. Allamand, V., & Guicheney, P. (2002). Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin). European Journal of Human Genetics, 10, 91–94. 3. Bertini, E., D’Amico, A., Gualandi, F., et al. (2011). Congenital muscular dystrophies: A brief review. Seminars in Pediatric Neurology, 18, 277–288. 4. Bharucha-Goebel, D. X., Santi, M., Medne, L., et al. (2013). Severe congenital RYR1-associated myopathy: The expanding clinicopathologic and genetic spectrum. Neurology, 80, 1584–1589. 5. Bonnemann, C. G., Wang, C. H., Quijano-roy, S., et al. (2014). Diagnostic approach to the congenital muscular dystrophies. Neuromuscular Disorders, 24, 289–311.
|
|