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Publications by Agoston Szel

The Expression of the Leber Congenital Amaurosis Protein AIPL1 Coincides With Rod and Cone Photoreceptor Development

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2003English

Related publications

The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations

Archives of Ophthalmology
2004English

Leber Congenital Amaurosis

2020English

Disruption of Intraflagellar Protein Transport in Photoreceptor Cilia Causes Leber Congenital Amaurosis in Humans and Mice

Cilia
Cell Biology
2012English

Molecular and Clinical Analysis of 27 German Patients With Leber Congenital Amaurosis

PLoS ONE
Multidisciplinary
2018English

Leber Congenital Amaurosis RPE65: 7 Years Follow Up

Gaceta Medica de Mexico
Medicine
2019English

Deletion of M-Opsin Prevents "M Cone" Degeneration in a Mouse Model of Leber Congenital Amaurosis

2019English

Mutation Screen of the TUB Gene in Patients With Retinitis Pigmentosa and Leber Congenital Amaurosis

Experimental Eye Research
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2006English

Hypomorphic Mutations Identified in the Candidate Leber Congenital Amaurosis Gene CLUAP1

Genetics in Medicine
MedicineGenetics
2016English

Nonpenetrance of the Most Frequent Autosomal Recessive Leber Congenital Amaurosis Mutation inNMNAT1

JAMA Ophthalmology
Ophthalmology
2014English

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