Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis

Neurology

Volumn 80, Issue 19, 2013, Pages 1771-1777

  Cannon, Ashley ^a   Fujioka, Shinsuke ^a,b   Rutherford, Nicola J ^a   Ferman, Tanis J ^b   Broderick, Daniel F ^b   Boylan, Kevin B ^b   Graff Radford, Neill R ^b   Uitti, Ryan J ^b   Rademakers, Rosa ^a   Wszolek, Zbigniew K ^b   Dickson, Dennis W ^a  

^a MAYO GRADUATE SCHOOL   (United States)

^b MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TAR DNA BINDING PROTEIN;

ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; ATYPICAL EXTRAPYRAMIDAL DISORDER; AUTOPSY; CASE REPORT; EXTRAPYRAMIDAL SYNDROME; FEMALE; FRONTAL VARIANT FRONTOTEMPORAL DEMENTIA; GENE; GENETIC VARIABILITY; GRN GENE; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MISSENSE MUTATION; MOTONEURON; ORGAN WEIGHT; PHENOTYPE; PRIORITY JOURNAL; SPINAL CORD NERVE CELL;

AGED; AMYOTROPHIC LATERAL SCLEROSIS; BASAL GANGLIA DISEASES; BRAIN; FEMALE; FRONTOTEMPORAL DEMENTIA; GENETIC VARIATION; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MIDDLE AGED; MUTATION, MISSENSE;

EID: 84879092067     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3182919059     Document Type: Article

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