Oates, E., Rossor, A., Hafezparast, M., Gonzalez, M., Speziani, F., MacArthur, D., . . . Reilly, M. (2013). Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia. Elsevier.
Citação norma ChicagoOates, Emily C., et al. Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia. Elsevier, 2013.
MLA citiranjeOates, Emily C., et al. Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia. Elsevier, 2013.
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