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year={2014},
title={Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association},
journal={KIDNEY INTERNATIONAL},
volume={85},
number={6},
pages={1310-1317},
document_type={Article},
} 

@ARTICLE{
author={Bogdanovic Radovan M|,Kuburovic Vladimir|,Stajic Natasa|,Mughal S|,Hilger A|,Ninic Sanja S|,Prijic Sergej M|0000-0002-2175-6611,Ludwig Michael|},
year={2012},
title={Liddle syndrome in a Serbian family and literature review of underlying mutations},
journal={EUROPEAN JOURNAL OF PEDIATRICS},
volume={171},
number={3},
pages={471-478},
document_type={Review},
} 

@ARTICLE{
author={Bogdanovic Radovan M|,Draaken Markus|,Toromanovic Alma|,Djordjevic Maja S|,Stajic Natasa|,Ludwig Michael|},
year={2010},
title={A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency},
journal={PEDIATRIC NEPHROLOGY},
volume={25},
number={11},
pages={2363-2368},
document_type={Article},
} 

@ARTICLE{
author={Pavicevic Snezana|,Bogdanovic Radovan M|,Ludwig Michael|,Samardzic Mira P|},
year={2008},
title={Dent Disease},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={136},
number={},
pages={312-315},
document_type={Article},
}