Subject Areas on Research
- Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.
- Obesity and diabetes genetic variants associated with gestational weight gain.
- Pathology of inherited manganese transporter deficiency.
- Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man.