Nesin, V., Wiley, G., Kousi, M., Ong, E., Lehmann, T., Nicholl, D. J., . . . Tsiokas, L. (2014). Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis. National Academy of Sciences.
Chicago Stili AlıntıNesin, Vasyl, et al. Activating Mutations in STIM1 and ORAI1 Cause Overlapping Syndromes of Tubular Myopathy and Congenital Miosis. National Academy of Sciences, 2014.
MLA AlıntıNesin, Vasyl, et al. Activating Mutations in STIM1 and ORAI1 Cause Overlapping Syndromes of Tubular Myopathy and Congenital Miosis. National Academy of Sciences, 2014.
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