Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

James S. Friedman, Joseph W. Ray, Naushin Waseem, Kory Johnson, Matthew J. Brooks, Therése Hugosson, Debra Breuer, Kari E. Branham, Daniel S. Krauth, Sara J. Bowne, Lori S. Sullivan, Vesna Ponjavic, Lotta Gränse, Ritu Khanna, Edward H. Trager, Linn M. Gieser, Dianna Hughbanks-Wheaton, Radu I. Cojocaru, Noor M. Ghiasvand, Christina F. ChakarovaMagnus Abrahamson, Harald H. H. Goering, Andrew R. Webster, David G. Birch, Goncalo R. Abecasis, Yang Fann, Shomi S. Bhattacharya, Stephen P. Daiger, John R. Heckenlively, Sten Andréasson, Anand Swaroop

Ophthalmology, Lund
Division of Clinical Chemistry and Pharmacology

Research output: Contribution to journal › Article › peer-review

1 Doctoral Thesis (compilation)

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2018

Electrophysiology - when nothing is seen
Hugosson, T., 2018, Lund: Lund University: Faculty of Medicine. 61 p.
Research output: Thesis › Doctoral Thesis (compilation)

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Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

Research output

Search results

Electrophysiology - when nothing is seen