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pro vyhledávání: '"Gotzl, J."'
Autor:
Gotzl, J., Colombo, Alessio Vittorio, Mazaheri, Fargol, Smith, S., Fellerer, K., Butovsky, O., Tahirovic, Sabina, Capell, A., Haass, Christian
Publikováno v:
Journal of neurochemistry 138(Supplement 1), 410 (2016).
Heterozygous loss-of-function mutations in the progranulin(GRN) gene result in GRN haploinsufficiency, which is a majorcause for familial frontotemporal lobar degeneration (FTLD) withTAR DNA-binding protein (TDP) -43 and ubiquitin-positiveinclusions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10678::4b6634e911b3a8176aea1f360bdfb8ea
https://pub.dzne.de/record/145519
https://pub.dzne.de/record/145519
