top of page
KOR
CONTACT
HOME
COMPANY
NEWS
TECHNOLOGY
R&D
QUALITY
SERVICES
Prenatal
Neonatal
Health Checkup
Rare Disease
Precision Oncology
CONTACT
More
Use tab to navigate through the menu items.
De novo mutations in COL4A5 identified by whole exome sequencing in 2 girls with Alport syndrome in Korea.
bottom of page