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Publications by Bianca Haase
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
Strong Selection for Behavioural Resilience in Australian Stock Working Dogs Identified by Selective Sweep Analysis
Canine Genetics and Epidemiology
Related publications
Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children
JAMA Ophthalmology
Ophthalmology
Congenital Stationary Night Blindness
Cav1.4 IT Mouse as Model for Vision Impairment in Human Congenital Stationary Night Blindness Type 2
Channels
Medicine
Biochemistry
Biophysics
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 Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
American Journal of Human Genetics
Genetics
Night-Blindness and Vitamin A
BMJ
Night-Blindness
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Congenital Blindness and Visual Impairment Cause Infection or Non Infection
Materia Socio Medica