A novel mutation of SOD-1 (Gly 108 Val) in familial amyotrophic lateral sclerosis

European Journal of Neurology

Volumn 4, Issue 1, 1997, Pages 48-51

  Orrell, R W ^a,b,e   Habgood, J J ^a   Shepherd, D I ^c   Donnai, D ^a,d   De Belleroche, J ^a  

^a IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

^b CHARING CROSS HOSPITAL   (United Kingdom)

^c NORTH MANCHESTER GENERAL HOSPITAL   (United Kingdom)

^d ST MARY S HOSPITAL   (United Kingdom)

^e UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

Amyotrophic lateral sclerosis; Copper zinc superoxide dismutase; Genetics; Motor neuron disease; Mutation; SOD 1

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; ENDONUCLEASE; GLYCINE; VALINE;

ADULT; AGED; AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; CODON; EXON; FEMALE; GENE MUTATION; GENOTYPE; HETEROZYGOTE; HUMAN; MALE; ONSET AGE; PATHOGENICITY; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; TRANSGENIC ANIMAL;

EID: 0031027733     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1468-1331.1997.tb00298.x     Document Type: Article

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