Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)
Year: 1998
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/7.9.1517
Institution: University of Würzburg
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2126930913
