Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis [1]

Journal of Medical Genetics

Volumn 35, Issue 2, 1998, Pages 174-

  Hayward, C ^a   Brock, D J H ^a   Minns, R A ^a   Swingler, R J ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARAGINE; COPPER ZINC SUPEROXIDE DISMUTASE; DNA; SERINE;

ADOLESCENT; AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; CASE REPORT; CODON; DNA POLYMORPHISM; FEMALE; GENE MUTATION; HOMOZYGOSITY; HUMAN; LETTER; MUSCLE WEAKNESS; PHENOTYPE; PRIORITY JOURNAL;

EID: 0031960868     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (6)