DSpace at RU >

Browsing by Author Yau, K.S.

Full Text	Issue Date	Title	Author(s)
	2011	Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.	Sambuughin, N.; Yau, K.S.; Duff, R.M.; Bayarsaikhan, M.; Lu, S.J., et al
	2010	Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.	Sambuughin, N.; Yau, K.S.; Olive, M.; Duff, R.M.; Bayarsaikhan, M., et al