Estañ, M. C., Fernández-Núñez, E., Zaki, M. S., Esteban, M. I., Donkervoort, S., Hawkins, C., . . . Ruiz-Perez, V. L. (2019). Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy. Nat Commun.
Chicago-tyylinen lähdeviittausEstañ, María Cristina, et al. "Recessive Mutations in Muscle-specific Isoforms of FXR1 Cause Congenital Multi-minicore Myopathy." Nat Commun 2019.
MLA-viiteEstañ, María Cristina, et al. "Recessive Mutations in Muscle-specific Isoforms of FXR1 Cause Congenital Multi-minicore Myopathy." Nat Commun 2019.
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