Počet záznamov: 1
Disruption of exonic splicing enhancer elements is the principal cause of exon skipping associated with seven nonsense or missense alleles of NF1
Názov Disruption of exonic splicing enhancer elements is the principal cause of exon skipping associated with seven nonsense or missense alleles of NF1 Autor Zaťková Andrea 1971- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV SCOPUS RID ORCID Spoluautori Messiaen L. Vandenbroucke I Wieser R. Fonatsch C. Krainer A.R. Wimmer Katherine Zdroj.dok. Human Mutation. Vol. 24, iss. 6 (2004), p.491-501 Jazyk dok. eng - angličtina Krajina US - Spojené štáty Druh dok. rozpis článkov z periodík (rbx) Ohlasy AUCLAIR, J. - BUISINE, M.P. - NAVARRO, C. - RUANO, E. - MONTMAIN, G. - DESSEIGNE, F. - SAURIN, J.C. - LASSET, C. - BONADONA, V. - GIRAUD, S. - PUISIEUX, A. - WANG, Q. Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing. In HUMAN MUTATION. ISSN 1059-7794, FEB 2006, vol. 27, no. 2, p. 145-154. 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Kategória ADMB - Vedecké práce v zahraničných neimpaktovaných časopisoch registrovaných vo WOS Core Collection alebo SCOPUS Kategória (od 2022) V3 - Vedecký výstup publikačnej činnosti z časopisu Typ výstupu článok Rok vykazovania 2004 Registrované v WOS Registrované v SCOPUS Registrované v CCC DOI 10.1002/humu.20103 
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