Analysis of indel variations in the human disease-associated genes CDKN2AIP, WDR66, USP20 and OR7C2 in a Korean population.
- Resource Type
- Article
- Source
Journal of Genetics . Dec2014 Supplement, Vol. 93, p1-11. 11p.- Subject
- *
HUMAN genes
*GENETIC polymorphisms
*GENETIC disorders
*DISEASES
*DELETION mutation - Language
- ISSN
- 0022-1333