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.
Stile di citazione ChicagoNesin, Vasyl, et al. Activating Mutations in STIM1 and ORAI1 Cause Overlapping Syndromes of Tubular Myopathy and Congenital Miosis. National Academy of Sciences, 2014.
Citazione MLANesin, 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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