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    Feinstein, M., Flusser, H., Lerman-Sagie, T., Ben-Zeev, B., Lev, D., Agamy, O., Cohen, I., Kadir, R., Sivan, S., Leshinsky-Silver, E., Markus, B., & Birk, O. S. (2014). vPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2). Journal of medical genetics, 51(5), 303–308. http://access.bl.uk/ark:/81055/vdc_100135140157.0x000032
  
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