Cita APA

Sambuughin, N., Yau, K. S., Olivé, M., Duff, R. M., Bayarsaikhan, M., Lu, S., . . . Goldfarb, L. G. (2010). Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores. Elsevier.

Chicago Style Citation

Sambuughin, Nyamkhishig, et al. Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy With Cores. Elsevier, 2010.

Cita MLA

Sambuughin, Nyamkhishig, et al. Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy With Cores. Elsevier, 2010.