Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1

Ivan Prokudin, Cas Simons, John R. Grigg, Rebecca Storen, Vikrant Kumar, Zai Y. Phua, James Smith, Maree Flaherty, Sonia Davila, Robyn V. Jamieson*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

55 Citations (Scopus)

Fingerprint

Dive into the research topics of 'Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1'. Together they form a unique fingerprint.

Medicine & Life Sciences