Title : Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies - Dohrn_2017_J.Neurochem_143_507 |
Author(s) :
Dohrn MF , Glockle N , Mulahasanovic L , Heller C , Mohr J , Bauer C , Riesch E , Becker A , Battke F , Hortnagel K , Hornemann T , Suriyanarayanan S , Blankenburg M , Schulz JB , Claeys KG , Gess B , Katona I , Ferbert A , Vittore D , Grimm A , Wolking S , Schols L , Lerche H , Korenke GC , Fischer D , Schrank B , Kotzaeridou U , Kurlemann G , Drager B , Schirmacher A , Young P , Schlotter-Weigel B , Biskup S |
Ref :
Journal of Neurochemistry , 143 :507 , 2017 |
Abstract : Dohrn_2017_J.Neurochem_143_507 |
ESTHER : Dohrn_2017_J.Neurochem_143_507 |
PubMedSearch : Dohrn_2017_J.Neurochem_143_507 |
PubMedID: 28902413 |
Gene_locus related to this paper:
human-NDRG1 |