Erratum: Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores (The American Journal of Human Genetics (2010) 87 (842-847))
Journal article published in 2011 by
N. Sambuughin,
K. S. Yau,
M. Olivé,
R. M. Duff,
M. Bayarsaikhan,
S. Lu,
L. Gonzalez-Mera,
P. Sivadorai,
K. J. Nowak,
G. Ravenscroft 
,
F. L. Mastaglia,
K. N. North,
B. Ilkovski,
H. Kremer,
M. Lammens
and other authors.
,
F. L. Mastaglia,
K. N. North,
B. Ilkovski,
H. Kremer,
M. Lammens
and other authors.
