Molecular BiologybioRxivPreprint
Molecular basis for a novel systemic form of human hereditary apoA-I amyloidosis with vision loss
Isabel M Morgado, Pierre-Raphaël Rothschild, Afra Panahi…·Sophie Valleix
The paper identifies a novel form of hereditary apoA-I amyloidosis caused by Glu34Lys mutation, revealing structural changes that lead to amyloid formation and vision loss.
DOI 10.1101/354001