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المؤلفون: Daman Kumari, Bruce E. Hayward, Karen Usdin, Antonia G. Vitalo, Ricardo Mouro Pinto, Xiao-Nan Zhao, Geum-Yi Kim, Carson J. Miller
المصدر: Journal of Huntington's Disease
مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Huntingtin, Ataxia, Somatic cell, Review, Biology, base excision repair, DNA Mismatch Repair, non-homologous end-joining, Genomic Instability, 03 medical and health sciences, Cellular and Molecular Neuroscience, Exon, FMR1-associated disorders, Mice, 0302 clinical medicine, Huntington's disease, medicine, Huntingtin Protein, trinucleotide repeat instability, Animals, Humans, Genetics, Genes, Modifier, Fragile X-related disorders, Polyglutamine tract, medicine.disease, mismatch repair, 030104 developmental biology, Huntington Disease, Friedreich ataxia, Fragile X Syndrome, double-strand break repair, Neurology (clinical), medicine.symptom, Trinucleotide repeat expansion, Trinucleotide Repeat Expansion, 030217 neurology & neurosurgery, Huntington’s disease
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f399a5de4f0187afd3e05d67e00613beTest
http://europepmc.org/articles/PMC7990428Test -
2دورية أكاديمية
المؤلفون: Zhao, Xiaonan, Kumari, Daman, Miller, Carson J., Kim, Geum-Yi, Hayward, Bruce, Vitalo, Antonia G., Pinto, Ricardo Mouro, Usdin, Karen, Jones, Lesley, Pearson, Christopher E., Wheeler, Vanessa
المصدر: Journal of Huntington's Disease; 2021, Vol. 10 Issue 1, p149-163, 15p
مصطلحات موضوعية: HUNTINGTON disease, SPINOCEREBELLAR ataxia, ANIMAL disease models, HUNTINGTIN protein, ATAXIA, DISEASES