Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome.

Solassol, Jérôme

Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome. [electronic resource] - Human mutation 06 2019 - 716-720 p. digital

Publication Type: Journal Article

1098-1004

10.1002/humu.23725 doi


Adult
Alu Elements
Colorectal Neoplasms, Hereditary Nonpolyposis--genetics
Exons
Female
Genetic Predisposition to Disease
High-Throughput Nucleotide Sequencing
Humans
Male
MutL Protein Homolog 1--genetics
Mutagenesis, Insertional
Pedigree
Phenotype
Sequence Analysis, DNA--methods