A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
Genome Med
; 11(1): 48, 2019 07 26.
Article
in En
| MEDLINE
| ID: mdl-31349857
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Predisposition to Disease
/
Polymorphism, Single Nucleotide
/
Genome-Wide Association Study
/
Exome Sequencing
/
Mosaicism
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Genome Med
Year:
2019
Document type:
Article
Affiliation country:
Country of publication: