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Naslov Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD) (Article)
Autori Fatehi F Okhovat AA Nilipour Y Mroczek M Straub V Topf A Palibrk Aleksa Peric Stojan Z  Rakocevic-Stojanovic Vidosava M Najmabadi H Nafissi S 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2020), vol. 27 br. 11, str. 2257-2266
Projekat Sanofi Genzyme; Ultragenyx; LGMD2I Research Fund; Samantha J Brazzo Foundation; LGMD2D Foundation; Kurt + Peter Foundation; Muscular Dystrophy UK; Coalition to Cure Calpain 3; National Human Genome Research InstituteUnited States Department of Health & Hu
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Two novel mutations in the FHL1 gene extending the phenotypic spectrum (Meeting Abstract)
Autori Strehle E Johnson Katherine Rakocevic-Stojanovic Vidosava M Peric Stojan Z  Farrugia M Longman C Straub V 
Info NEUROMUSCULAR DISORDERS, (2017), vol. 27 br. , Suppl. 2, str. S138-S139
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort (Meeting Abstract)
Autori Tonf A Nikodinovic-Glumac Jelena Peric Stojan Z  Cassop-Thompson M Bertoli M Johnson Katherine Phillips L MacArthur D Rakocevic-Stojanovic Vidosava M Straub V 
Info NEUROMUSCULAR DISORDERS, (2016), vol. 26 br. , Suppl. 2, str. S113-S114
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations (Meeting Abstract)
Autori Johnson Katherine Bertoli M Phillips L Toepf A Claeys K Rakocevic-Stojanovic Vidosava M Peric Stojan Z  Vissine J Hahn Andreas Maddison P Akay E Bastian A Lusakowska A Lek M Xu L MacArthur D Straub V 
Info NEUROMUSCULAR DISORDERS, (2016), vol. 26 br. , Suppl. 2, str. S108-S109
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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