SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis

Annals of Neurology

Volumn 70, Issue 6, 2011, Pages 867-870

  Fecto, Faisal ^a   Siddique, Teepu ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; COPPER ZINC SUPEROXIDE DISMUTASE; SIGMAR1 PROTEIN; UNCLASSIFIED DRUG;

AMYOTROPHIC LATERAL SCLEROSIS; AUTOSOMAL DOMINANT DISORDER; CELLULAR DISTRIBUTION; CHROMOSOME 9P; CHROMOSOME SEGREGATION; ENDOPLASMIC RETICULUM STRESS; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HUMAN; NEUROPATHOLOGY; NONHUMAN; ONSET AGE; PATHOGENESIS; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROGRESSIVE BULBAR PALSY; PROGRESSIVE PONTOBULBAR PALSY; REVIEW; RNA PROCESSING;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, SIGMA;

EID: 84255175951     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.22648     Document Type: Review

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