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Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2
Rossor, A. M., Oates, E. C., Salter, H. K., Liu, Y., Murphy, S. M., Schule, R., Gonzalez, M. A., Scoto, M., Phadke, R., Sewry, C. A., Houlden, H., Jordanova, A., Tournev, I., Chamova, T., Litvinenko,Volume:
138
Language:
english
Journal:
Brain
DOI:
10.1093/brain/awu356
Date:
February, 2015
File:
PDF, 1.74 MB
english, 2015