Australia’s first snapshot of families at risk of blindness from rare genetic eye disease

Multiple tumors without kinship occur simultaneously in the small intestine in neuroendocrine cancer
5 November 2021
Potential brain mechanism underlying chronic neuropathic pain in individuals with HIV
5 November 2021

Australia’s first snapshot of families at risk of blindness from rare genetic eye disease

New research has revealed for the first time the number of Australian families affected by genetic mutations that cause the rare genetic eye disease Leber Hereditary Optic Neuropathy (LHON) – and the risk of going blind from the disease.

Comments are closed.