Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients
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30. Apr. 2018
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Online veröffentlicht: 30. Apr. 2018
Seitenbereich: 110 - 118
DOI: https://doi.org/10.2478/enr-2018-0013
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© 2018 Daniel Danis et al., published by De Gruyter Open
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Danis, Daniel
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of SciencesBratislava, Slovakia
Brennerova, Katarina
Department of Paediatrics, Medical Faculty, Comenius University, Children Faculty HospitalBratislava, Slovakia
Skopkova, Martina
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of SciencesBratislava, Slovakia
Kurdiova, Timea
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of SciencesBratislava, Slovakia
Ukropec, Jozef
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of SciencesBratislava, Slovakia
Stanik, Juraj
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of SciencesBratislava, Slovakia
Department of Paediatrics, Medical Faculty, Comenius University, Children Faculty HospitalBratislava, Slovakia
Kolnikova, Miriam
Department of Pediatric Neurology, Medical Faculty, Comenius University, Children Faculty HospitalBratislava, Slovakia
Gasperikova, Daniela
Institute of Experimental Endocrinology, Biomedical Research Center, Slovak Academy of SciencesBratislava, Slovakia