Cargando…
Corrigendum to “Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles”
Autores principales: | Kamakari, Smaragda, Kokkinou, Vassiliki, Koutsodontis, George, Stamatiou, Polixeni, Giatzakis, Christoforos, Anastasakis, Anastasios, Aslanides, Ioannis Minas, Koukoula, Stavrenia, Panagiotoglou, Theoni, Datseris, Ioannis, Tsilimbaris, Miltiadis K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311797/ https://www.ncbi.nlm.nih.gov/pubmed/30647958 http://dx.doi.org/10.1155/2018/3039672 |
Ejemplares similares
-
Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles
por: Smaragda, Kamakari, et al.
Publicado: (2018) -
First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation
por: Kamakari, Smaragda, et al.
Publicado: (2014) -
An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease
por: Mäkeläinen, Suvi, et al.
Publicado: (2019) -
ABCA4 mutations in Portuguese Stargardt patients: identification of new mutations and their phenotypic analysis
por: Maia-Lopes, Susana, et al.
Publicado: (2009) -
Subretinal Fibrosis in Stargardt's Disease with Fundus Flavimaculatus and ABCA4 Gene Mutation
por: Rossi, Settimio, et al.
Publicado: (2012)