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المؤلفون: Stojan Perić, Vladana Marković, Ayşe Candayan, Els De Vriendt, Nikola Momčilović, Andrija Savić, Nataša Dragašević-Mišković, Marina Svetel, Zorica Stević, Ivo Božović, Šarlota Mesaroš, Jelena Drulović, Ivana Basta, Igor Petrović, Olivera Tamaš, Milija Mijajlović, Ivana Novaković, Dragoslav Sokić, Albena Jordanova
المصدر: Cells; Volume 11; Issue 18; Pages: 2804
Cellsمصطلحات موضوعية: Spastin, DNA Copy Number Variations, Spastic Paraplegia, Hereditary, Kinesins, Membrane Transport Proteins, Proteins, Neural Cell Adhesion Molecule L1, General Medicine, Genetic Heterogeneity, Phenotype, hereditary spastic paraplegia, genetic testing, pure HSP, complicated HSP, Humans, Human medicine, Prospective Studies, Biology, Serbia
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7554198faa8da26227606fb0b437717Test
https://pubmed.ncbi.nlm.nih.gov/36139378Test -
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المؤلفون: Jovan Pešović, Stojan Perić, Miloš Brkušanin, Goran Brajušković, Vidosava Rakočević-Stojanović, Dušanka Savić-Pavićević
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, lcsh:QH426-470, Somatic cell, Buccal swab, 030105 genetics & heredity, Biology, Myotonic dystrophy, Instability, Disease course, 03 medical and health sciences, 0302 clinical medicine, repeat interruptions, CTG expansion, Internal medicine, medicine, Genetics, In patient, Genetics (clinical), Original Research, somatic instability, medicine.disease, lcsh:Genetics, myotonic dystrophy 1, Endocrinology, Molecular Medicine, age at onset, 030217 neurology & neurosurgery, DMPK
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4da371df27913c05afed3d54995ca0e8Test
http://europepmc.org/articles/PMC6278776Test