Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions - Roehl, Angelika C; Vogt, Julia; Mussotter, Tanja; Zickler, Antje N; Spöti, Helene; Högel, Josef; Chuzhanova, Nadia A; Wimmer, Katharina; Kluwe, Lan; Mautner, Victor-Felix; Cooper, David N; Kehrer-Sawatzki, Hildegard (Human mutation, 2010)
Keywords: Alu; Carrier Proteins - genetics; Chromosomes, Human, Pair 17 - genetics; Computational Biology; Genes, Neurofibromatosis 1; Humans; microdeletion; Microsatellite Repeats - genetics; Mitosis - genetics; mitotic nonallelic homologous recombination; NAHR; Neurofibromatosis 1 - genetics; neurofibromatosis type 1; Neurofibromin 1 - genetics; NF1; non-B DNA; Nuclear Proteins - genetics; Oligonucleotide Array Sequence Analysis - methods; Polycomb Repressive Complex 2; Polymorphism, Single Nucleotide; Recombination, Genetic; Sequence Deletion; tumorigenesis