D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.

Human mutation

Volumn 20, Issue 6, 2002, Pages 473-

  Parton, Matthew J ^a   Broom, Wendy ^a   Andersen, Peter M ^a   Al Chalabi, Ammar ^a   Nigel Leigh, P ^a   Powell, John F ^a   Shaw, Christopher E ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MICROSATELLITE DNA; SUPEROXIDE DISMUTASE;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CHEMISTRY; ENZYMOLOGY; FAMILY HEALTH; FEMALE; FOUNDER EFFECT; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HAPLOTYPE; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; RECESSIVE GENE;

AMINO ACID SUBSTITUTION; AMYOTROPHIC LATERAL SCLEROSIS; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; FOUNDER EFFECT; GENES, RECESSIVE; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MICROSATELLITE REPEATS; PEDIGREE; POLYMORPHISM, GENETIC; SUPEROXIDE DISMUTASE;

EID: 0036885011     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9081     Document Type: Article

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