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

Autor:	J M, Hartikainen, M M, Pirskanen, A H, Arffman, U K, Ristonmaa, A J, Mannermaa
Rok vydání:	1999
Předmět:	Ovarian Neoplasms Amino Acid Substitution BRCA1 Protein RNA Splicing Molecular Sequence Data Humans Breast Neoplasms Female Frameshift Mutation Polymerase Chain Reaction Finland Polymorphism Restriction Fragment Length Chromosomes Human Pair 17
Zdroj:	Human mutation. 15(1)
ISSN:	1098-1004
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::c78364d52fdc5ca398777a247eba5e32 https://pubmed.ncbi.nlm.nih.gov/10980533 Zobrazit plný text záznamu Plný text