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Authors: Ginjaar, IB Kneppers, ALJ von der Meulen, JDM Anderson, LVB Bremmer-Bout, M van Deutekom, JCT Weegenaar, J den Dunnen, JT Bakker, E
Citation: Ib. Ginjaar et al., Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family, EUR J HUM G, 8(10), 2000, pp. 793-796
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