Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.
Clin Genet
; 87(6): 536-42, 2015 Jun.
Article
in En
| MEDLINE
| ID: mdl-25318681
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ethnicity
/
Colorectal Neoplasms, Hereditary Nonpolyposis
/
Founder Effect
/
DNA-Binding Proteins
/
Mutation
Type of study:
Diagnostic_studies
/
Etiology_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
America do norte
Language:
En
Journal:
Clin Genet
Year:
2015
Document type:
Article
Affiliation country:
España
Country of publication:
Dinamarca