Zhou, H., Lillis, S., Loy, R. E., Ghassemi, F., Rose, M. R., Norwood, F., . . . Jungbluth, H. (2010). Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene.
Citação norma ChicagoZhou, Haiyan, et al. Multi-minicore Disease and Atypical Periodic Paralysis Associated With Novel Mutations in the Skeletal Muscle Ryanodine Receptor (RYR1) Gene. 2010.
Citação norma MLAZhou, Haiyan, et al. Multi-minicore Disease and Atypical Periodic Paralysis Associated With Novel Mutations in the Skeletal Muscle Ryanodine Receptor (RYR1) Gene. 2010.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.