A Novel Compound Heterozygous Best1 Gene Mutation in Two Siblings Causing Autosomal Recessive Bestrophinopathy

AuthID
 P-00X-N9B
6
Author(s)
Haque, OI
·
Chandrasekaran, A
·
Document Type
Article
Year published
2022
Published
in BMC OPHTHALMOLOGY
Volume: 22, Issue: 1
Indexing
Wos®
Scopus®
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Publication Identifiers
Pubmed: 36527004
Scopus: 2-s2.0-85144132443
Wos: WOS:000899770100001
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