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Publications by Britta Baumann

Cone Dystrophy With Supernormal Rod Response Is Strictly Associated With Mutations inKCNV2

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2008English

Related publications

Homozygosity Mapping in Patients With Cone–Rod Dystrophy: Novel Mutations and Clinical Characterizations

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2010English

Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1995English

A Deletion in Nephronophthisis 4 (NPHP4) Is Associated With Recessive Cone-Rod Dystrophy in Standard Wire-Haired Dachshund

Genome Research
Genetics
2008English

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

2020English

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Rod-Cone Dystrophy in Spinocerebellar Ataxia Type 1

Archives of Ophthalmology
2011English

Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family

Acta Ophthalmologica
MedicineOphthalmology
2018English

Cone Dystrophy in Patient With HomozygousRP1L1Mutation

BioMed Research International
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
2015English

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