Cargando…
Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract
Autores principales: | Zhu, Yanan, Yu, Hao, Wang, Wei, Gong, Xiaohua, Yao, Ke |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430210/ https://www.ncbi.nlm.nih.gov/pubmed/25970271 http://dx.doi.org/10.1371/journal.pone.0125949 |
Ejemplares similares
-
A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract
por: Zhu, Yanan, et al.
Publicado: (2014) -
Novel mutation of GJA8 in autosomal dominant congenital cataracts
por: Ding, Ning, et al.
Publicado: (2020) -
Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
por: Micheal, Shazia, et al.
Publicado: (2018) -
Identification of a Missense Mutation in GJA8 Gene in an Iranian Family with Autosomal Dominant Congenital Cataract
por: Asghari, Mahla, et al.
Publicado: (2023) -
A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family
por: Wang, Kaijie, et al.
Publicado: (2009)