Familial ALS is associated with mutations in all exons of SOD1: A novel mutation in exon 3 (Gly72Ser)

Journal of the Neurological Sciences

Volumn 153, Issue 1, 1997, Pages 46-49

  Orrell, R W ^a,b   Marklund, S L ^c   Debelleroche, J S ^a  

^a IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

^b CHARING CROSS HOSPITAL   (United Kingdom)

^c UMEÅ UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Amyotrophic lateral sclerosis; Familial; Genetics; Mutation; Progressive muscular atrophy; SOD1

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CASE REPORT; EXON; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HUMAN; MALE; MOTOR NEURON DISEASE; MUSCLE ATROPHY; PEDIGREE ANALYSIS; POINT MUTATION; PRIORITY JOURNAL;

AMYOTROPHIC LATERAL SCLEROSIS; CHROMOSOMES, HUMAN, PAIR 21; EXONS; HUMANS; MALE; MIDDLE AGED; POINT MUTATION; SUPEROXIDE DISMUTASE;

EID: 0031443762     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(97)00181-0     Document Type: Article

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