Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias

Human Molecular Genetics

Volumn 5, Issue 12, 1996, Pages 1887-1892

  Stevanin, Giovanni ^a   Trottier, Yvon ^b   Cancel, Géraldine ^a   Dürr, Alexandra ^a   David, Gilles ^a   Didierjean, Olivier ^a   Bürk, Katrin ^c   Imbert, Georges ^b   Saudou, Frederic ^b   Abada Bendib, Myriem ^a,d   Gourfinkel An, Isabelle ^a   Benomar, Ali ^e   Abbas, Nacer ^a   Klockgether, Thomas ^c   Grid, Djamel ^f,g   Agid, Yves ^a   Mandel, Jean Louis ^b   Brice, Alexis ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d Ben Aknoun Hospital   (Algeria)

^e Hop des Spécialités   (Morocco)

^f CHU Mustapha   (Algeria)

^g GÉNÉTHON   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMINE; MUTANT PROTEIN; REPETITIVE DNA; TRINUCLEOTIDE;

AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN CORTEX; CEREBELLAR ATAXIA; CONTROLLED STUDY; FEMALE; GENE MUTATION; GENE SEGREGATION; HUMAN; HUMAN CELL; LYMPHOBLAST; MACHADO JOSEPH DISEASE; MAJOR CLINICAL STUDY; MALE; MARKER GENE; ONSET AGE; PRIORITY JOURNAL; PROTEIN ANALYSIS; SPINOCEREBELLAR DEGENERATION;

ATAXIA;

EID: 10544253082     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.12.1887     Document Type: Article

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