Neurofibromatosis type 2 in an infant presenting with visual impairment confirmed by genetic mutation analysis. Retina 2005;25(7):938-40
Date
10/06/2005Pubmed ID
16205576DOI
10.1097/00006982-200510000-00019Scopus ID
2-s2.0-26844437172 (requires institutional sign-in at Scopus site) 2 CitationsAuthor List
Kim JE, Ruttum MSMESH terms used to index this publication - Major topics in bold
Chromosomes, Human, Pair 22DNA Mutational Analysis
Exons
Fluorescein Angiography
Genes, Neurofibromatosis 2
Humans
Infant
Male
Neurofibromatosis 2
Point Mutation
Polymerase Chain Reaction
Vision Disorders
