R. L. Albin

Absence of Mutation in the {beta}- and {gamma}-Synuclein Genes in Familial Autosomal Dominant Parkinson's Disease (1998)

Lavedan, C., Buchholtz, S., Auburger, G., Albin, R. L., Athanassiadou, A., Blancato, J., ...

Fuch's corneal dystrophy in a patient with mitochondrial DNA mutations.

Albin, R L

A patient with Fuch's corneal dystrophy, sensorineural hearing loss, diabetes, cardiac conduction defects, ataxia, and hyperreflexia is described. Analysis of lymphocyte mitochondrial DNA showed...