Haplotype analysis and ancient origin of the BRCA1 c.4035delA Baltic founder mutation

التفاصيل البيبلوغرافية
العنوان: Haplotype analysis and ancient origin of the BRCA1 c.4035delA Baltic founder mutation
المؤلفون: Bing Jian Feng, Laima Tihomirova, Vilius Rudaitis, Ramunas Janavicius, David E. Goldgar, Laimonas Griskevicius, Silvija Ozolina
المصدر: European journal of medical genetics. 56(3)
سنة النشر: 2012
مصطلحات موضوعية: Genetic Markers, Maximum likelihood, Ubiquitin-Protein Ligases, Biology, Russia, Genetics, medicine, Cluster Analysis, Humans, Genetic Predisposition to Disease, Founder mutation, Genetics (clinical), Genetic testing, Likelihood Functions, medicine.diagnostic_test, Haplotype, Lithuania, General Medicine, Latvia, humanities, Founder Effect, Haplotypes, Mutation (genetic algorithm), Mutation, Gene pool, Poland, geographic locations
الوصف: Uncertainty exists about the origin of BRCA1 c.4035delA mutation which is prevalent in Baltic countries, with the highest frequency being in Lithuania (53% of all BRCA1 mutations), although formal founder mutation analysis by haplotype has not yet been undertaken. In this study we genotyped 78 unrelated BRCA1 c.4035delA mutation carriers families from Lithuania, Latvia, Poland and Russia. The results from the haplotype analyses were used to estimate the age of the mutation. Using maximum likelihood methods we estimated that the mutation arose approximately 1550 years (62 generations of 25 years) ago (ca. 5th century) somewhere in the present territory of Lithuania, in the area inhabited by ancient Baltic tribes at that time. Our results show that this mutation gradually entered the gene pool in the neighboring countries.
تدمد: 1878-0849
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::275df4eb7610d3ce11a939ba6993416bTest
https://pubmed.ncbi.nlm.nih.gov/23274591Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....275df4eb7610d3ce11a939ba6993416b
قاعدة البيانات: OpenAIRE