Cav1.4 IT Mouse as Model for Vision Impairment in Human Congenital Stationary Night Blindness Type 2

Channels - United States
doi 10.4161/chan.26368
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Informa UK Limited

Related search

Congenital Stationary Night Blindness

2020English

Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children

JAMA Ophthalmology
Ophthalmology
2018English

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

BioMed Research International
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
2018English

Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

PLoS ONE
Multidisciplinary
2013English

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

American Journal of Human Genetics
Genetics
2012English

Congenital Stationary Night Blindness With Hypoplastic Discs, Negative Electroretinogram and Thinning of the Inner Nuclear Layer

Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2016English

Tunnel Vision and Night Blindness in a 52-Year-Old Man

Medical Journal of Australia
Medicine
2011English

Night-Blindness

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1919English

A Mouse Model of Beta-Cell Dysfunction as Seen in Human Type 2 Diabetes

Journal of Diabetes Research
EndocrinologyMetabolismDiabetes
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy