Ergebnisse einschränken
Dokumententyp
Institution
Spezialsammlung
Sprache
- Englisch (5)
Autor
- Senderek, Jan (5)
- Stendel, Claudia (3)
- Chrast, Roman (2)
- Janecke, Andreas R. (2)
- Roos, Andreas (2)
- Sidiropoulos, Páris N. M. (2)
- Suter, Ueli (2)
- Antonellis, Anthony (1)
- Arnaud, Estelle (1)
- Auer-Grumbach, Michaela (1)
- Auer-Grumbach, Piet (1)
- Baets, Jonathan (1)
- Baudis, Michael (1)
- Bauer, Peter (1)
- Baumann, Reto (1)
- Beg, Asim A. (1)
- Benedicenti, Francesco (1)
- Beth Griffin, Laurie (1)
- Bornemann, Antje (1)
- Budka, Herbert (1)
- Claeys, Kristl G. (1)
- De Jonghe, Peter (1)
- Deconinck, Tine (1)
- Dufke, Andreas (1)
- El Shabrawi-Caelen, Laila (1)
- Ferbert, Andreas (1)
- Fink-Puches, Regina (1)
- Finkel, Richard S. (1)
- Fröhlich, Eleonore (1)
- Goebel, Hans H. (1) Mehr Weniger
Schlagwort
- Original Articles (5)
- 1070 (1)
- CMT (1)
- Charcot-Marie-Tooth disease (1)
- Charcot-Marie-Tooth neuropathy (1)
- Frabin/Fgd4 (1)
- Marinesco-Sjögren syndrome (1)
- RNA processing (1)
- Rab11 (1)
- Rho-GTPase Cdc42 (1)
- SH3TC2 / KIAA1985 (1)
- SIL1 mutation (1)
- Schwann cell myelination (1)
- age-related macular degeneration (1)
- ataxia (1)
- cataract (1)
- cutis laxa (1)
- fibulin-5 (1)
- hereditary motor and sensory neuropathies (1)
- hereditary motor and sensory neuropathy (1)
- molecular genetics (1)
- myelination (1)
- myopathy (1)
- neurodegeneration (1)
- neuropathy (1)
- recycling endosome (1)
- whole-exome sequencing (1) Mehr Weniger