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Title : SERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large family - Roeben_2018_J.Med.Genet_55_39 |
Author(s) : Roeben B , Schule R , Ruf S , Bender B , Alhaddad B , Benkert T , Meitinger T , Reich S , Bohringer J , Langhans CD , Vaz FM , Wortmann SB , Marquardt T , Haack TB , Krageloh-Mann I , Schols L , Synofzik M |
Ref : Journal of Medical Genetics , 55 :39 , 2018 |
Abstract : Roeben_2018_J.Med.Genet_55_39 |
ESTHER : Roeben_2018_J.Med.Genet_55_39 |
PubMedSearch : Roeben_2018_J.Med.Genet_55_39 |
PubMedID: 28916646 |
Gene_locus related to this paper: human-SERAC1 |
Title : Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa - Muller_2008_Child.Adolesc.Psychiatry.Ment.Health_2_33 |
Author(s) : Muller TD , Reichwald K , Bronner G , Kirschner J , Nguyen TT , Scherag A , Herzog W , Herpertz-Dahlmann B , Lichtner P , Meitinger T , Platzer M , Schafer H , Hebebrand J , Hinney A |
Ref : Child Adolesc Psychiatry Ment Health , 2 :33 , 2008 |
Abstract : Muller_2008_Child.Adolesc.Psychiatry.Ment.Health_2_33 |
ESTHER : Muller_2008_Child.Adolesc.Psychiatry.Ment.Health_2_33 |
PubMedSearch : Muller_2008_Child.Adolesc.Psychiatry.Ment.Health_2_33 |
PubMedID: 19014633 |
Title : Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans - Gschwendtner_2008_Stroke_39_1593 |
Author(s) : Gschwendtner A , Ripke S , Freilinger T , Lichtner P , Muller-Myhsok B , Wichmann HE , Meitinger T , Dichgans M |
Ref : Stroke , 39 :1593 , 2008 |
Abstract : Gschwendtner_2008_Stroke_39_1593 |
ESTHER : Gschwendtner_2008_Stroke_39_1593 |
PubMedSearch : Gschwendtner_2008_Stroke_39_1593 |
PubMedID: 18323494 |