Published in
Wiley, European Journal of Neurology, 7(14), p. 819-822, 2007
DOI: 10.1111/j.1468-1331.2007.01808.x
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A unique case of limb-girdle muscular dystrophy type 2A carrying novel compound heterozygous mutations in the human CAPN3 gene
Journal article published in 2007 by
E. Matsubara,
A. Tsuchiya,
N. Minami,
I. Nishino 
,
M. A. Pappolla,
M. Shoji,
K. Abe
,
M. A. Pappolla,
M. Shoji,
K. Abe
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