Alteraciones maculares en aniridia congénita

Author:

Casas-Llera P.,Ruiz-Casas D.,Alió J.L.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference30 articles.

1. Ocular and nonocular findings in patients with aniridia;Valenzuela;Can J Ophthalmol.,2004

2. Aniridia: current pathology and management;Lee;Acta Ophthalmol.,2008

3. Implication of non-coding PAX6 mutations in aniridia;Plaisancié;Hum Genet.,2018

4. Clinical and molecular aspects of aniridia;Kokotas;Clin Genet.,2010

5. Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia;Dubey;Mol Vis.,2015

Cited by 4 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. A novel PAX6 variant as the cause of aniridia in a Chinese patient with SRRRD;BMC Medical Genomics;2023-08-04

2. Gene expression and regulation relative to specific tissues and functions;The Regulatory Genome in Adaptation, Evolution, Development, and Disease;2023

3. La aniridia: un desafío multidisciplinar para la oftalmología de nuestro tiempo;Archivos de la Sociedad Española de Oftalmología;2021-11

4. Aniridia: A multidisciplinary challenge for ophthalmology in our times;Archivos de la Sociedad Española de Oftalmología (English Edition);2021-11

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