Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene

Di Huang, Dan Zhang, Shang Chih Chen, May Thandar Aung-Htut, Tina M. Lamey, Jennifer A. Thompson, Terri L. McLaren, John N. De Roach, Sue Fletcher, Steve D. Wilton, Fred K. Chen, Samuel McLenachan

Research output: Contribution to journal › Article › peer-review

1 Active
2 Finished

3 results

Active

Accelerating the identification and treatment of splice-altering mutations underlying inherited retinal diseases
Chen, F., Fletcher, S., McLenachan, S. & Cunningham, P.
National Health & Medical Research Council NHMRC
1/01/20 → 31/12/24
Project: Research
Finished

MRFF - Developing Personalised Treatment for Retinal Degeneration
Chen, F.
National Health & Medical Research Council NHMRC
1/01/18 → 31/12/21
Project: Research
From discovery to therapy in genetic eye diseases
Mackey, D., Craig, J., Hewitt, A., Burdon, K., Jamieson, R., Grigg, J., MacGregor, S., Chen, F., Otlowski, M. & Schofield, D.
National Health & Medical Research Council NHMRC
1/01/16 → 31/12/20
Project: Research