(PDF) Mutation in the Intracellular Chloride Channel CLCC1

Mutation in the Intracellular Chloride Channel CLCC1 Associated With Autosomal Recessive Retinitis Pigmentosa

PLoS Genetics - United States

doi 10.1371/journal.pgen.1007504

Related search

A Novel NR2E3 Gene Mutation in Autosomal Recessive Retinitis Pigmentosa With Cystic Maculopathy

Acta Ophthalmologica

English

Mutation Screening of Multiple Genes in Spanish Patients With Autosomal Recessive Retinitis Pigmentosa by Targeted Resequencing

Multidisciplinary

English

High Prevalence of Mutations in theEYSGene in Japanese Patients With Autosomal Recessive Retinitis Pigmentosa

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

Missense Mutation in the USH2A Gene: Association With Recessive Retinitis Pigmentosa Without Hearing Loss

American Journal of Human Genetics

English

Mutations in USH2A in Spanish Patients With Autosomal Recessive Retinitis Pigmentosa: High Prevalence and Phenotypic Variation

Journal of Medical Genetics

English

Whole Exome Sequencing Identified Novel CRB1 Mutations in Chinese and Indian Populations With Autosomal Recessive Retinitis Pigmentosa

Scientific Reports

Multidisciplinary

English

Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

NMNAT1 Mutation Causing Retinitis Pigmentosa

Acta Ophthalmologica

English

Mesangioproliferative Glomerulonephritis Associated With Retinitis Pigmentosa.

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English