Amanote Research
Register
Sign In
Correction:Unilateral Retinitis Pigmentosa Occurring in an Individual With a Mutation in the CLRN1 Gene
BMJ Case Reports
- United Kingdom
doi 10.1136/bcr-2017-222045corr1
Full Text
Open PDF
Abstract
Available in
full text
Categories
Medicine
Date
April 28, 2018
Authors
Unknown
Publisher
BMJ
Related search
A Novel NR2E3 Gene Mutation in Autosomal Recessive Retinitis Pigmentosa With Cystic Maculopathy
Acta Ophthalmologica
Medicine
Ophthalmology
Novel Mutation in ABCC6 Gene in a Japanese Pedigree With Pseudoxanthoma Elasticum and Retinitis Pigmentosa
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Missense Mutation in the USH2A Gene: Association With Recessive Retinitis Pigmentosa Without Hearing Loss
American Journal of Human Genetics
Genetics
NMNAT1 Mutation Causing Retinitis Pigmentosa
Acta Ophthalmologica
Medicine
Ophthalmology
Mutation Screen of the TUB Gene in Patients With Retinitis Pigmentosa and Leber Congenital Amaurosis
Experimental Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Mutation in the Intracellular Chloride Channel CLCC1 Associated With Autosomal Recessive Retinitis Pigmentosa
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Mutation Analysis of the RPGR Gene Reveals Novel Mutations in South European Patients With X-Linked Retinitis Pigmentosa
European Journal of Human Genetics
Genetics
Polypoidal Choroidal Vasculopathy in a Case With Retinitis Pigmentosa
International Ophthalmology
Ophthalmology
Rhodopsin Mutations in Chinese Patients With Retinitis Pigmentosa
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular