Sambuughin, N., Yau, K. S., Olivé, M., Duff, R. M., Bayarsaikhan, M., Lu, S., . . . Goldfarb, L. G. (2011). Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores. Elsevier.
シカゴスタイル引用形Sambuughin, Nyamkhishig, et al. Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy With Cores. Elsevier, 2011.
MLA引用形式Sambuughin, Nyamkhishig, et al. Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy With Cores. Elsevier, 2011.
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