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1 Ergebnisse
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Frequent genes in rare diseases: panel-based next generatio..:
Dohrn, Maike F.
;
Glöckle, Nicola
;
Mulahasanovic, Lejla
...
Journal of Neurochemistry. 143 (2017) 5 - p. 507-522 , 2017
Link:
https://doi.org/10.1111/jnc.14217
RT Journal T1
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_jnc.14217&Exemplar=1&LAN=DE A1 Dohrn, Maike F. A1 Glöckle, Nicola A1 Mulahasanovic, Lejla A1 Heller, Corina A1 Mohr, Julia A1 Bauer, Christine A1 Riesch, Erik A1 Becker, Andrea A1 Battke, Florian A1 Hörtnagel, Konstanze A1 Hornemann, Thorsten A1 Suriyanarayanan, Saranya A1 Blankenburg, Markus A1 Schulz, Jörg B. A1 Claeys, Kristl G. A1 Gess, Burkhard A1 Katona, Istvan A1 Ferbert, Andreas A1 Vittore, Debora A1 Grimm, Alexander A1 Wolking, Stefan A1 Schöls, Ludger A1 Lerche, Holger A1 Korenke, G. Christoph A1 Fischer, Dirk A1 Schrank, Bertold A1 Kotzaeridou, Urania A1 Kurlemann, Gerhard A1 Dräger, Bianca A1 Schirmacher, Anja PB Wiley YR 2017 SN 0022-3042 JF Journal of Neurochemistry VO 143 IS 5 SP 507 OP 522 LK http://dx.doi.org/https://doi.org/10.1111/jnc.14217 DO https://doi.org/10.1111/jnc.14217 SF ELIB - SuUB Bremen
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