Autori: Teran Natasa
Naslov | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study (Meeting Abstract) |
Autori | Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Skrjanec-Pusenjak Marusa Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1390-1390 |
Projekat | [P3-0326] |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study (Meeting Abstract) |
Autori | Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Pusenjak Marusa Skrjanec Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1390-1390 |
Projekat | [P3-0326] |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study (Article) |
Autori | Vodnjov Nina Toplisek Janez Maver Ales Cuturilo Goran Jaklic Helena Teran Natasa Visnjar Tanja Skrjanec Pusenjak Marusa Hodzic Alenka Miljanovic Olivera Peterlin Borut Writzl Karin Mahdieh Nejat |
Info | PLOS ONE, (2023), vol. 18 br. 12, str. - |
Projekat | Slovenian Research and Innovation Agency [P3-0326] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans (Meeting Abstract) |
Autori | Maver Ales Kovanda Anja Bergant Gaber Teran Natasa Vrecar Irena Brankovic Marija ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 292-292 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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