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2017
Mark Genotype and Phenotype in an unusual form of Laurence-Moon-Bardet-Biedl syndrome
Kamme, Christina ; Mayer, Anja Kathrin ; Strom, Tim M. ; Andréasson, Sten ^LU and Weisschuh, Nicole (2017) In Acta Ophthalmologica 95(3). p.250-252
- Contribution to journal › Article
2016
Mark NEK1 mutations in familial amyotrophic lateral sclerosis.
Brenner, David ; Müller, Kathrin ; Wieland, Thomas ; Weydt, Patrick ; Böhm, Sarah ; Lulé, Dorothée ; Hübers, Annemarie ; Neuwirth, Christoph ; Weber, Markus and Borck, Guntram , et al. (2016) In Brain 139(5).
- Contribution to journal › Letter
Mark Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
Weisschuh, Nicole ; Mayer, Anja K ; Strom, Tim M ; Kohl, Susanne ; Glöckle, Nicola ; Schubach, Max ; Andréasson, Sten ^LU ; Bernd, Antje ; Birch, David G and Hamel, Christian P , et al. (2016) In PLoS ONE 11(1).
- Contribution to journal › Article