TY  - JOUR
AU  - Molina-Solana, Pedro
AU  - Morillo-Sánchez, María José
AU  - Méndez-Vidal, Cristina
AU  - Ramos-Jiménez, Manuel
AU  - Domínguez-Serrano, Borja
AU  - Antiñolo, Guillermo
AU  - Rodríguez-de-la-Rúa-Franch, Enrique
PY  - 2021
DO  - 10.5935/0004-2749.20210064
UR  - http://hdl.handle.net/10668/17807
T2  - Arquivos brasileiros de oftalmologia
AB  - Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been associated with mutations in this gene. We describe an observational case report of an unusual clinical phenotype of Stargardt...
LA  - en
KW  - ATP-Binding Cassette Transporters
KW  - Electroretinography
KW  - Female
KW  - Fluorescein Angiography
KW  - Humans
KW  - Middle Aged
KW  - Mutation
KW  - Phenotype
KW  - Stargardt Disease
KW  - Tomography, Optical Coherence
TI  - Unusual clinical phenotype of Stargardt disease.
TY  - research article
VL  - 84
ER  -