학술논문
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies
Document Type
Article
Author
Dohrn, M.F.; Glöckle, N.; Mulahasanovic, L.; Heller, C.; Mohr, J.; Bauer, C.; Riesch, E.; Becker, A.; Battke, F.; Hörtnagel, K.; Biskup, S.; Schulz, J.B.; Gess, B.; Hornemann, T.; Suriyanarayanan, S.; Blankenburg, M.; Claeys, K.G.; Katona, I.; Ferbert, A.; Vittore, D.; Grimm, A.; Wolking, S.; Schöls, L.; Lerche, H.; Korenke, G.C.; Fischer, D.; Schrank, B.; Kotzaeridou, U.; Kurlemann, G.; Dräger, B.; Schirmacher, A.; Young, P.; Schlotter-Weigel, B.
Source
In: Journal of Neurochemistry . (Journal of Neurochemistry, December 2017, 143(5):507-522)
Subject
Language
English
ISSN
14714159
00223042
00223042