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Browsing by Author Olive, M.
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Author(s)
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
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