M. Caballero

Two novel mutations in the Norrie disease gene associated with the classical ocular phenotype.

L. Hesse, A. Gal, B. Schroeder, 1996, Ophthalmic genetics.

Autoantibody screening in Guillain–Barré syndrome

I. Rojas-Marcos, R. Rojas-García, I. Illa, 2021, medRxiv.

Characterization of human immunodeficiency virus type 1 vif gene in long-term asymptomatic individuals.

H. Agut, B. Autran, I. Agostini, 2000, Virology.

A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie disease.

M. Salcedo, A. Gal, H. Wedemann, 1994, Human molecular genetics.