Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias

Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias. Fournier, C., Anquetil, V., Camuzat, A., Stirati-Buron, S., Sazdovitch, V., Molina-Porcel, L., Turbant, S., Rinaldi, D., Sánchez-Valle, R., Barbier, M., Latouche, M., Neuro-CEB Neuropathology Network, Stevanin, G., Seilhean, D., Brice, A., Duyckaerts, C., & Le Ber, I. Acta Neuropathologica Communications, 6(1):41, May, 2018.
doi bibtex

@article{fournier_interrupted_2018,
	title = {Interrupted {CAG} expansions in {ATXN2} gene expand the genetic spectrum of frontotemporal dementias},
	volume = {6},
	issn = {2051-5960},
	doi = {10.1186/s40478-018-0547-8},
	language = {eng},
	number = {1},
	journal = {Acta Neuropathologica Communications},
	author = {Fournier, Clémence and Anquetil, Vincent and Camuzat, Agnès and Stirati-Buron, Sandrine and Sazdovitch, Véronique and Molina-Porcel, Laura and Turbant, Sabrina and Rinaldi, Daisy and Sánchez-Valle, Raquel and Barbier, Mathieu and Latouche, Morwena and {Neuro-CEB Neuropathology Network} and Stevanin, Giovanni and Seilhean, Danielle and Brice, Alexis and Duyckaerts, Charles and Le Ber, Isabelle},
	month = may,
	year = {2018},
	pmid = {29848387},
	pmcid = {PMC5977499},
	keywords = {Aged, Humans, Magnetic Resonance Imaging, Female, Male, Middle Aged, Brain, Frontotemporal Dementia, Aged, 80 and over, Cohort Studies, Amyotrophic Lateral Sclerosis, Tomography, Emission-Computed, Single-Photon, Frontotemporal dementia, DNA-Binding Proteins, Corticobasal degeneration, Frontotemporal lobar degeneration, TDP-43, C9orf72, GRN, Trinucleotide Repeat Expansion, Amyotrophic lateral sclerosis, Ataxin 2, Ataxin-2, Corticobasal syndrome, SCA2},
	pages = {41}
}

Downloads: 0