| 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 |
| Gene_locus related to this paper: human-NDRG1 |
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 (2017)
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies
Journal of Neurochemistry
143 :507
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 (2017)
Journal of Neurochemistry
143 :507