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Publications by Claudia Schmuckermair

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

Channels
MedicineBiochemistryBiophysics
2013English

Related publications

Congenital Stationary Night Blindness

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Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children

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

BioMed Research International
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
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Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

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

American Journal of Human Genetics
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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
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Tunnel Vision and Night Blindness in a 52-Year-Old Man

Medical Journal of Australia
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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

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