TY  - JOUR
AU  - Herranz Martín, Saúl
AU  - Azzouz, Mimoun
PY  - 2017
DO  - 10.1242/dmm.029892
SN  - 1754-8411
SN  - 1754-8403
UR  - https://hdl.handle.net/20.500.14352/95721
T2  - Disease Models & Mechanisms
AB  - Intronic GGGGCC repeat expansions in C9orf72 are the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Two major pathologies stemming from the hexanucleotide RNA expansions (HREs) have been identified...
LA  - eng
M2  - 859
PB  - The Company of Biologists
KW  - C9orf72
KW  - Neurodegeneration
KW  - ALS/FTD
KW  - Mouse model
KW  - C9RAN aggregates
TI  - Viral delivery of C9ORF72 hexanucleotide repeat expansions in mice lead to repeat length dependent neuropathology and behavioral deficits
TY  - journal article
VL  - 10
ER  -