von Salomé, Jenny <br/><br/>
Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.  [electronic resource] 

 -  Familial cancer  10 2018 
 - 531-537 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1573-7292 
<br/><br/><label>Standard No.: </label>10.1007/s10689-017-0067-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Colorectal Neoplasms, Hereditary Nonpolyposis--genetics<br/>Female<br/>Finland<br/>Founder Effect<br/>Genetics, Population<br/>Haplotypes--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>MutL Protein Homolog 1--genetics<br/>Mutation, Missense<br/>Pedigree<br/>Sweden