@ARTICLE{
author={Johnson Katherine,...,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,...,(broj koautora 23)},
year={2019},
title={Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population},
journal={JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY},
volume={90},
number={4},
pages={490-+},
document_type={Letter},
} 

@ARTICLE{
author={Johnson Katherine,...,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,...,(broj koautora 17)},
year={2017},
title={Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness},
journal={ORPHANET JOURNAL OF RARE DISEASES},
volume={12},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Johnson Katherine,...,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,...,(broj koautora 21)},
year={2017},
title={Detection of TRIM32 variants associated with LGMD2H in a large cohort of patients with unexplained limb-girdle weakness},
journal={NEUROMUSCULAR DISORDERS},
volume={27},
number={},
pages={S142-S143},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Strehle E,Johnson Katherine,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Farrugia M,Longman C,Straub V},
year={2017},
title={Two novel mutations in the FHL1 gene extending the phenotypic spectrum},
journal={NEUROMUSCULAR DISORDERS},
volume={27},
number={},
pages={S138-S139},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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},
year={2016},
title={A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort},
journal={NEUROMUSCULAR DISORDERS},
volume={26},
number={},
pages={S113-S114},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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},
year={2016},
title={Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations},
journal={NEUROMUSCULAR DISORDERS},
volume={26},
number={},
pages={S108-S109},
document_type={Meeting Abstract},
}