S. Kubota

HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model.

R G Weleber, D. Hamasaki, T. Higashide, 2000, Investigative ophthalmology & visual science.

Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.

T. Higashide, F. Wong, G. Inana, 2007, Experimental eye research.

Changes in retinal synaptic proteins in the transgenic model expressing a mutant HRG4 (UNC119).

T. Higashide, G. Inana, A. Kobayashi, 2002, Investigative ophthalmology & visual science.

Truncation mutation in HRG4 (UNC119) leads to mitochondrial ANT-1-mediated photoreceptor synaptic and retinal degeneration by apoptosis.

T. Higashide, G. Inana, A. Kobayashi, 2006, Investigative ophthalmology & visual science.

Photoreceptor synaptic protein HRG4 (UNC119) interacts with ARL2 via a putative conserved domain

G. Inana, A. Kobayashi, S. Kubota, 2003, FEBS letters.