A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataract

Johanna L. Jones
, Mark A. Corbett
, Elise Yeaman
, Duran Zhao
, Jozef Gecz
, Robert J. Gasperini
, Jac C. Charlesworth
, David A. Mackey
, James E. Elder
, Jamie E. Craig
, Kathryn P. Burdon

Centre for Ophthalmology and Visual Science (affiliated with the Lions Eye Institute)

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

9 Citations (Scopus)

1 results

Finished

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