3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype.
| Autor: | Kekou, Kiriaki, Florentin, Lina, Metaxotou, Catherine |
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| Zdroj: | Human Mutation; 1998 Supplement, Vol. 11, pS209-S212, 4p |
| Databáze: | Complementary Index |
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