Comment: Double mutants of frontotemporal dementia genes-simple co-occurrence?

Neurology

Volumn 81, Issue 15, 2013, Pages 1338-

  Pastor, Pau ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

PROGRANULIN; TAU PROTEIN;

ALLELE; ENVIRONMENTAL FACTOR; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; MOTONEURON; MUTANT; NOTE; PENETRANCE; PRIORITY JOURNAL;

DNA REPEAT EXPANSION; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; NEURODEGENERATIVE DISEASES; PROTEINS;

EID: 84888245752     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3182a825a1     Document Type: Note

References (3)

1. van Blitterswijk M, Baker MC, De Jesus-Hernandez M, et al. C9ORF72 repeat expansions in cases with previously identified pathogenic mutations. Neurology 2013;81:1332-1341.
2. De Jesus-Hernandez M, Mackenzie IR, Boeve BF, et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011;72:245-256.
3. Renton AE, Majounie E, Waite A, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011;72:257-268.