Published in
Elsevier, Neuromuscular Disorders, 11(20), p. 709-711, 2010
DOI: 10.1016/j.nmd.2010.06.003
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Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin
Journal article published in 2010 by
Katharine Forrest,
Jemima E. Mellerio,
Stephanie Robb,
Patricia J. C. Dopping-Hepenstal,
John A. McGrath,
Lu Liu,
Stefan J. A. Buk,
Safa Al-Sarraj,
Elizabeth Wraige,
Heinz Jungbluth
This paper was not found in any repository, but could be made available legally by the author.
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