Loss of ERLIN2 function leads to juvenile primary lateral sclerosis

Annals of Neurology

Volumn 72, Issue 4, 2012, Pages 510-516

  Al Saif, Amr ^a   Bohlega, Saeed ^a   Al Mohanna, Futwan ^a  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; SHORT HAIRPIN RNA;

ADOLESCENT; ALS2 GENE; ANIMAL CELL; ARTICLE; CASE REPORT; CELL GROWTH; CHILD; CONTROLLED STUDY; DNA SEQUENCE; ENDOPLASMIC RETICULUM; ERLIN2 GENE; GENE; GENE MAPPING; GENE MUTATION; HOMOZYGOSITY; HUMAN; IN VITRO STUDY; LIPID RAFT; MOTONEURON; MOUSE; NONHUMAN; PRIMARY LATERAL SCLEROSIS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REAL TIME POLYMERASE CHAIN REACTION; RNA INTERFERENCE; SIGMAR1 GENE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; CELL COUNT; CELLS, CULTURED; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 8; DNA; ENDOPLASMIC RETICULUM-ASSOCIATED DEGRADATION; FEMALE; HUMANS; HYDROXYMETHYLGLUTARYL-COA-REDUCTASES, NADP-DEPENDENT; INFANT; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; MALE; MEMBRANE PROTEINS; MOTOR NEURON DISEASE; REAL-TIME POLYMERASE CHAIN REACTION; RNA INTERFERENCE; RNA SPLICE SITES; RNA, MESSENGER; SIGNAL TRANSDUCTION; TRANSFECTION;

EID: 84868091740     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.23641     Document Type: Article

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