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Kalbacher Hubert

πŸ‡£πŸ‡€ University of TΓΌbingen
ORCIDOpenAlex2 articles in GJC

2 articles in GJC

2.

OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retina.

Pesch Ulrike E A, Fries Julia E, Bette Stefanie, Kalbacher Hubert, Wissinger Bernd, Alexander Christiane et al.

Invest Ophthalmol Vis SciNov 200444 citationsBasic Science

OPA1, linked to dominant optic atrophy, was found specifically in retinal ganglion, starburst amacrine, and horizontal cells. This suggests OPA1 is crucial for retinal signal processing, not just optic nerve integrity.

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