Genetics of congenital cataract, its diagnosis and therapeutics-Reference-Cited by-同舟云学术

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Genetics of congenital cataract, its diagnosis and therapeutics

Published:2018-12 Issue:4 Volume:5 Page:252-257
ISSN:2314-808X
Container-title:Egyptian Journal of Basic and Applied Sciences
language:en
Short-container-title:Egyptian Journal of Basic and Applied Sciences

Author:

Khan Luqman¹,Shaheen Nargis²,Hanif Qaisar³,Fahad Shah²,Usman Muhammad⁴

Affiliation:

1. Graduate School of Life Sciences, Tohoku University, Sendai, Japan

2. Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan

3. Department of Ophthalmology Allied Hospital, Medical University, Faisalabad, Pakistan

4. Department of Bioinformatics & Computational Biology, Virtual University of Pakistan, Pakistan

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1016/j.ejbas.2018.07.001

Reference46 articles.

1. Molecular basis of glaucoma and its therapeutical analysis in Pakistan: an overview

2. Clinical and experimental advances in congenital and paediatric cataracts

3. Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)

4. The Use of Autozygosity Mapping and Next-Generation Sequencing in Understanding Anterior Segment Defects Caused by an Abnormal Development of the Lens

5. Comprehensive Mutational Screening in a Cohort of Danish Families with Hereditary Congenital Cataract

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Major intrinsic protein (MIP)/aquaporin 0 (AQP0) mRNA gene expression in congenital cataracts;Gazzetta Medica Italiana Archivio per le Scienze Mediche;2024-06

2. Transcriptome alterations in sf3b4-depleted zebrafish: Insights into cataract formation in retinitis pigmentosa model;Experimental Eye Research;2024-03

3. Expression of mRNA forkhead box protein e3 (FoxE3) in congenital cataracts: a cross-sectional study;Gazzetta Medica Italiana Archivio per le Scienze Mediche;2024-01

4. Mutational analysis of CRYAA gene of cataract and investigating risk assessment factors responsible for eye diseases in district Buner, KPK, Pakistan;Cellular and Molecular Biology;2023-09-30

5. Whole Exome Sequencing of 20 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Cataracts;International Journal of Molecular Sciences;2023-07-13

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