DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

American Journal of Human Genetics

Volumn 74, Issue 6, 2004, Pages 1128-1135

  Chen, Ying Zhang ^a   Bennett, Craig L ^a   Huynh, Huy M ^a   Blair, Ian P ^a   Puls, Imke ^c   Irobi, Joy ^d   Dierick, Ines ^d   Abel, Annette ^c   Kennerson, Marina L ^f,g   Rabin, Bruce A ^h   Nicholson, Garth A ^f,g   Auer Grumbach, Michaela ⁱ   Wagner, Klaus ⁱ   De Jonghe, Peter ^d,e   Griffin, John W ^h   Fischbeck, Kenneth H ^c   Timmerman, Vincent ^d   Cornblath, David R ^h   Chance, Phillip F ^a,b  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^d DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^e ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^f UNIVERSITY OF SYDNEY   (Australia)

^g Department of Microbiology and Infectious Diseases   (Australia)

^h JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

ⁱ UNIVERSITY OF GRAZ   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE; RNA HELICASE;

ADOLESCENT; ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 9Q; CLINICAL FEATURE; DISEASE COURSE; ENZYME ACTIVITY; GENE; GENE FUNCTION; GENE LOCUS; GENETIC CODE; HUMAN; HUMAN CELL; HUMAN TISSUE; IGHMBP2 GENE; LIFESPAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUSCLE ATROPHY; MUSCLE WEAKNESS; NERVE CELL DEGENERATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PYRAMIDAL SIGN; RENT1 GENE; RNA PROCESSING; SENSATION; SEQUENCE HOMOLOGY; SETX GENE;

EID: 2442658908     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/421054     Document Type: Article

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