Cargando…
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Pediatric cataract is a leading cause of childhood blindness. This study aimed to determine the genetic cause of pediatric cataract in Australian families by screening known disease-associated genes using massively parallel sequencing technology. We sequenced 51 previously reported pediatric catarac...
Autores principales: | Javadiyan, Shari, Craig, Jamie E., Souzeau, Emmanuelle, Sharma, Shiwani, Lower, Karen M., Mackey, David A., Staffieri, Sandra E., Elder, James E., Taranath, Deepa, Straga, Tania, Black, Joanna, Pater, John, Casey, Theresa, Hewitt, Alex W., Burdon, Kathryn P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633377/ https://www.ncbi.nlm.nih.gov/pubmed/28839118 http://dx.doi.org/10.1534/g3.117.300109 |
Ejemplares similares
-
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract
por: Javadiyan, Shari, et al.
Publicado: (2016) -
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)
por: Javadiyan, Shari, et al.
Publicado: (2017) -
Whole-exome sequencing prioritizes candidate genes for hereditary cataract in the Emory mouse mutant
por: Bennett, Thomas M, et al.
Publicado: (2023) -
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka
por: Javadiyan, Shari, et al.
Publicado: (2018) -
Pathogenic genetic variants identified in Australian families with paediatric cataract
por: Jones, Johanna L, et al.
Publicado: (2022)