P80 Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole exome analysis
Leidenroth, A, Sorte, H. Sørmo, Gilfillan, G, Ehrlich, M, Lyle, R, Hewitt, J.E
Published in Neuromuscular disorders : NMD (01.03.2012)
Published in Neuromuscular disorders : NMD (01.03.2012)
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Journal Article
P17 Investigating the molecular mechanisms of FSHD
Leidenroth, A, Hampson, A, Mitchell, L, Pollington, J, Vafadar-Isfahani, N, Hewitt, J
Published in Neuromuscular disorders : NMD (2010)
Published in Neuromuscular disorders : NMD (2010)
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Journal Article