A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation

Autor:	Arto Mannermaa, Ulla K. Ristonmaa, Mia Pirskanen, Airi H. Arffman, Jaana M. Hartikainen
Rok vydání:	2000
Předmět:	Genetics Exon Splice site mutation RNA splicing Mutation (genetic algorithm) splice Aberrant splicing Biology Acceptor Genetics (clinical) Frameshift mutation
Zdroj:	Human Mutation. 15:120-120
ISSN:	1098-1004 1059-7794
DOI:	10.1002/(sici)1098-1004(200001)15:1<120::aid-humu31>3.0.co;2-e
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9314fca48ca783067a29d4eb1d424325 https://doi.org/10.1002/(sici)1098-1004(200001)15:1<120::aid-humu31>3.0.co Zobrazit plný text záznamu Plný text