Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele.

Neurology

Volumn 70, Issue 9, 2008, Pages 666-676

  Niemann, S ^a   Landers, J E ^a   Churchill, M J ^a   Hosler, B ^a   Sapp, P ^a   Speed, W C ^a   Lahn, B T ^a   Kidd, K K ^a   Brown Jr , R H ^a   Hayashi, Y ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NR3B NMDA RECEPTOR; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CASE CONTROL STUDY; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; HAPLOTYPE; HUMAN; MOTONEURON; MOTOR NEURON DISEASE; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PHYSIOLOGY; POPULATION GENETICS; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MOTOR NEURON DISEASE; MOTOR NEURONS; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, N-METHYL-D-ASPARTATE; SUPEROXIDE DISMUTASE;

EID: 40349101680     PISSN: None     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000271078.51280.17     Document Type: Article

References (0)