Clinically early-stage CSPα mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss

Acta neuropathologica communications

Volumn 3, Issue , 2015, Pages 73-

  Benitez, Bruno A ^a   Cairns, Nigel J ^a   Schmidt, Robert E ^a   Morris, John C ^a   Norton, Joanne B ^a   Cruchaga, Carlos ^a   Sands, Mark S ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE STRING PROTEIN; GLIAL FIBRILLARY ACIDIC PROTEIN; HEAT SHOCK PROTEIN 40; MEMBRANE PROTEIN; SYNAPTOPHYSIN;

ADULT; AGED; BRAIN; DNA MUTATIONAL ANALYSIS; FEMALE; GENE EXPRESSION REGULATION; GENETICS; HUMAN; MALE; METABOLISM; MIDDLE AGED; MUTATION; NERVE CELL; NEURONAL CEROID LIPOFUSCINOSIS; PATHOLOGY; TRANSMISSION ELECTRON MICROSCOPY; ULTRASTRUCTURE; VERY ELDERLY;

ADULT; AGED; AGED, 80 AND OVER; BRAIN; DNA MUTATIONAL ANALYSIS; FEMALE; GENE EXPRESSION REGULATION; GLIAL FIBRILLARY ACIDIC PROTEIN; HSP40 HEAT-SHOCK PROTEINS; HUMANS; MALE; MEMBRANE PROTEINS; MICROSCOPY, ELECTRON, TRANSMISSION; MIDDLE AGED; MUTATION; NEURONAL CEROID-LIPOFUSCINOSES; NEURONS; SYNAPTOPHYSIN;

EID: 84966339419     PISSN: None     EISSN: 20515960     Source Type: Journal    
DOI: 10.1186/s40478-015-0256-5     Document Type: Article

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