Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies
Sutton, Ian J, Mocroft, A Paul, Lindley, Victoria H, Barber, Richard M, Bryon, R Jane, Winer, John B, MacDonald, Fiona
Published in Neuromuscular disorders : NMD (01.12.2004)
Published in Neuromuscular disorders : NMD (01.12.2004)
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