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
·
Tipo de Documento
Article
Year published
2022
Publicado
in BMC OPHTHALMOLOGY
Volume: 22, Número: 1
Indexing
Wos®
Scopus®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 36527004
SCOPUS: 2-s2.0-85144132443
Wos: WOS:000899770100001
Export Publication Metadata
Lista Marked
 Adicionar à lista Marked
Info
At this moment we don't have any links to full text documens.

Um espaço para investigadores e suas Instituições

Links Úteis

Ajuda

© 2024 CRACS & Inesc TEC - All Rights Reserved Política de Privacidade | Terms of Service