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- Meitinger, Thomas
- Strom, Tim M 3
- Andersen, Peter M 2
- Danzer, Karin M 2
- Ludolph, Albert C 2
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5 Einträge gefunden
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SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden
- Yilmaz, Rüstem
- Müller, Kathrin
- Brenner, David
- Volk, Alexander E
- Borck, Guntram
- Hermann, Andreas
- Meitinger, Thomas
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Exom-Sequenzierung bei Kindern:Ungeklärte Entwicklungsstörungen und neurologische Erkrankungen, Exome Sequencing in Children: Undiagnosed Developmental Delay and Neurological Illness
- Mahler, Elisa A
- Johannsen, Jessika
- Tsiakas, Konstantinos
- Kloth, Katja
- Lüttgen, Sabine
- Mühlhausen, Chris
- Alhaddad, Bader
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Mutations in the deubiquitinase gene USP8 cause Cushing's disease
- Reincke, Martin
- Sbiera, Silviu
- Hayakawa, Akira
- Theodoropoulou, Marily
- Osswald, Andrea
- Beuschlein, Felix
- Meitinger, Thomas
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Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.
- Linsel-Nitschke, Patrick
- Heeren, Jörg
- Aherrahrou, Zouhair
- Bruse, Petra
- Gieger, Christian
- Illig, Thomas
- Prokisch, Holger