Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases is a research paper published in Genes (2023). On theSindex it has a DataRank of 0. It has been cited 10 times.
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National Eye Institute
Grant: EY022356
National Eye Institute
Grant: EY018571
National Eye Institute
Grant: EY002520
National Eye Institute
Grant: P30EY010572
National Eye Institute
Grant: EY030499
National Eye Institute
Grant: S10OD023469
National Institutes of Health
Grant: 1S10OD023469-01
High Throughput Genomic Sequencer at BCM Core Facility
National Institutes of Health
Grant: 5R01EY022356-07
Molecular Basis of Human Visual System Disorders
National Institutes of Health
Grant: 1R01EY030499-01
Antisense therapy for the treatment of visual loss in Usher syndrome
National Institutes of Health
Grant: 5P30EY002520-40
P30 - Core Grant for Vision Research
National Institutes of Health
Grant: 5R01EY018571-03
Genetics of Early Onset Retinal Diseases
National Institutes of Health
Grant: 3P30EY010572-20S1
OPHTHALMOLOGY CORE FACILITY
FWCI
0.93
Citation Percentile
0.7%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals