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Naslov The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS) (Meeting Abstract)
Autori Peterlin AM Maver Ales Hodzic A Sega S Drulovic Jelena S  Novakovic Ivana V  Pekmezovic Tatjana D  Ristic S Kapovic Miljenko Peterlin B 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 400-400
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice (Article)
Autori Tumiene B Maver Ales Writzl Karin Hodzic A Cuturilo Goran Kuzmanic-Samija Radenka Culic V Peterlin Borut 
Info CLINICAL GENETICS, (2018), vol. 93 br. 5, str. 1057-1062
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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