FTLD/ALS as TDP-43 proteinopathies

Clinical Neurology

Volumn 50, Issue 11, 2010, Pages 1022-1024

  Ishihara, Tomohiko ^a   Ariizumi, Yuko ^a   Shiga, Atsushi ^a   Yokoseki, Akio ^a   Sato, Tatsuya ^a   Toyoshima, Yasuko ^a   Kakita, Akiyoshi ^a   Takahashi, Hitoshi ^a   Nishizawa, Masatoyo ^a   Onodera, Osamu ^a  

^a NIIGATA UNIVERSITY   (Japan)

Author keywords

ALS; FTLD; FTLD MND; TDP 43; Tdp 43 proteinopathy

Indexed keywords

TAR DNA BINDING PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; CELL INCLUSION; CLINICAL FEATURE; CONFERENCE PAPER; FAMILIAL DISEASE; FRONTAL LOBE; FRONTOTEMPORAL DEMENTIA; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MOTONEURON; NEUROPATHOLOGY; PATHOGENESIS; PHENOTYPE; TDP 43 PROTEINOPATHY; TEMPORAL LOBE;

AMYOTROPHIC LATERAL SCLEROSIS; DNA-BINDING PROTEINS; FRONTOTEMPORAL LOBAR DEGENERATION; HUMANS; INCLUSION BODIES; MUTATION; TDP-43 PROTEINOPATHIES;

EID: 84863048829     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: 10.5692/clinicalneurol.50.1022     Document Type: Conference Paper

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