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Por Brownell, A Keith W, Atkins, Chloe, Whiteley, Andrea, Woollard, Robert F, Kornelsen, Jude
Publicado no BMJ Open (2016)
Obter o texto integralPublicado no BMJ Open (2016)
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Myofibrillar myopathy due to TTN mutation in a Canadian family sharing the British founder haplotype
Por Pfeffer, Gerald, Joseph, Jeffrey T., Innes, A. Micheil, Frizzell, J. Bevan, Wilson, Ian J., Brownell, A. Keith W., Chinnery, Patrick F.
Publicado no Can J Neurol Sci (2014)
Obter o texto integralPublicado no Can J Neurol Sci (2014)
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