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

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• Finished

  Accelerating the identification and treatment of splice-altering mutations underlying inherited retinal diseases

  Chen, F. (Investigator 01), Fletcher, S. (Investigator 02), McLenachan, S. (Investigator 03) & Cunningham, P. (Investigator 04)

  NHMRC National Health and Medical Research Council

  1/01/20 → 31/12/24

  Project: Research

• MRFF - Developing Personalised Treatment for Retinal Degeneration

  Chen, F. (Investigator 01)

  NHMRC National Health and Medical Research Council

  1/01/18 → 31/12/21

  Project: Research

• From discovery to therapy in genetic eye diseases

  Mackey, D. (Investigator 01), Craig, J. (Investigator 02), Hewitt, A. (Investigator 03), Burdon, K. (Investigator 04), Jamieson, R. (Investigator 05), Grigg, J. (Investigator 06), MacGregor, S. (Investigator 07), Chen, F. (Investigator 08), Otlowski, M. (Investigator 09) & Schofield, D. (Investigator 10)

  NHMRC National Health and Medical Research Council

  1/01/16 → 31/12/20

  Project: Research