Mohr J

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 :

PubMedSearch : Dohrn_2017_J.Neurochem_143_507

PubMedID: 28902413

Gene_locus related to this paper: human-NDRG1

Title : Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cells - Eiberg_1986_Hum.Genet_74_174

Author(s) : Eiberg H , Mohr J

Ref : Hum Genet , 74 :174 , 1986

Abstract :

PubMedSearch : Eiberg_1986_Hum.Genet_74_174

PubMedID: 3770744

Mohr J

References (2)

1. Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies - Dohrn_2017_J.Neurochem_143_507

2. Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cells - Eiberg_1986_Hum.Genet_74_174