1. Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2. Issue 5 (14th August 2018) Authors: Laššuthová, P.; Vill, K.; Erdem‐Ozdamar, S.; Schröder, J.M.; Topaloglu, H.; Horvath, R.; Müller‐Felber, W.; Bansagi, B.; Schlotter‐Weigel, B.; Gläser, D.; Neupauerová, J.; Sedláčková, L.; Staněk, D.; Mazanec, R.; Weis, J.; Seeman, P.; Senderek, J. Journal: Clinical genetics Issue: Volume 94:Issue 5(2018) Page Start: 467 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Unusual congenital demyelinating neuropathies with sensory organ deficits caused by mutant transcription factors. (June 2017) Authors: Bansagi, B.; Duff, J.; Turnbull, D.; Horvath, R. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e236 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗