Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Atrophy and CRX[original query] |
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De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients. Ophthalmic genetics 2015 Mar 36 (1): 21-6. Zou Xuan, Yao Fengxia, Liang Xiaofang, Xu Fei, Li Hui, Sui Ruifang, Dong Fangti |
Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies. International journal of molecular sciences 2019 10 20 (19): . Boulanger-Scemama Elise, Mohand-Saïd Saddek, El Shamieh Said, Démontant Vanessa, Condroyer Christel, Antonio Aline, Michiels Christelle, Boyard Fiona, Saraiva Jean-Paul, Letexier Mélanie, Sahel José-Alain, Zeitz Christina, Audo Isabel |
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