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Retinitis

Distilling a Visual Network of Retinitis Pigmentosa Gene-Protein Interactions to Uncover New Disease Candidates

Daniel Boloc, Sergio Castillo-Lara, [ ... ], Josep F. Abril

Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned

Berta Almoguera, Jiankang Li, [ ... ], Carmen Ayuso

Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families

Sundaramurthy Srilekha, Tharigopala Arokiasamy, [ ... ], Nagasamy Soumittra

Subretinal Fluid in Eyes with Active Ocular Toxoplasmosis Observed Using Spectral Domain Optical Coherence Tomography

Yanling Ouyang, Fuqiang Li, [ ... ], Uwe Pleyer

Genotypic and Phenotypic Characterization of P23H Line 1 Rat Model

Elise Orhan, Deniz Dalkara, [ ... ], Isabelle Audo

Effect of Purified Murine NGF on Isolated Photoreceptors of a Rodent Developing Retinitis Pigmentosa

Maria Luisa Rocco, Bijorn Omar Balzamino, [ ... ], Luigi Aloe

Homogeneity Test for Correlated Binary Data

Changxing Ma, Guogen Shan, Song Liu

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

Zied Riahi, Crystel Bonnet, [ ... ], Christine Petit

Homozygosity Mapping and Targeted Sanger Sequencing Reveal Genetic Defects Underlying Inherited Retinal Disease in Families from Pakistan

Maleeha Maria, Muhammad Ajmal, [ ... ], Frans P. M. Cremers

Distribution and Determinants of Cytomegalovirus Induced End Organ Disease/s among People Living with HIV/AIDS in a Poor Resource Setting: Observation from India

Avirup Chakraborty, Tanmay Mahapatra, [ ... ], Nilanjan Chakraborty

Exome Sequencing Reveals Novel and Recurrent Mutations with Clinical Significance in Inherited Retinal Dystrophies

María González-del Pozo, Cristina Méndez-Vidal, [ ... ], Guillermo Antiñolo

Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa

Bastian Linder, Anja Hirmer, [ ... ], Utz Fischer

Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa

Satoshi Katagiri, Masakazu Akahori, [ ... ], Takeshi Iwata

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