Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Nature Genetics

Volumn 36, Issue 3, 2004, Pages 225-227

  Moreira, Maria Céu ^a   Klur, Sandra ^a   Watanabe, Mitsunori ^b   Németh, Andrea H ^c   Le Ber, Isabelle ^d   Moniz, José Carlos ^e   Tranchant, Christine ^f   Aubourg, Patrick ^g   Tazir, Meriem ^h   Schöls, Lüdger ⁱ   Pandolfo, Massimo ^j   Schulz, Jörg B ^k   Pouget, Jean ^l   Calvas, Patrick ^m   Shizuka Ikeda, Masami ^b   Shoji, Mikio ^b   Tanaka, Makoto ^b   Izatt, Louise ⁿ   Shaw, Christopher E ^o   M'Zahem, Abderrahim ^p   Dunne, Eimear ^c   Bomont, Pascale ^a   Benhassine, Traki ^q   Bouslam, Naïma ^d   Stevanin, Giovanni ^d   Brice, Alexis ^d   Guimarães, João ^r   Mendonça, Pedro ^s   Barbot, Clara ^t,u   Coutinho, Paula ^t,v   Sequeiros, Jorge ^t   Dürr, Alexandra ^d   Warter, Jean Marie ^f   Koenig, Michel ^a   more..

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

^b GUNMA UNIVERSITY   (Japan)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e HOSPITAL DE SANTO ANTÓNIO DOS CAPUCHOS   (Portugal)

^f UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^g HÔPITAL SAINT VINCENT DE PAUL   (France)

^h CHU Mustapha   (Algeria)

ⁱ ST JOSEF HOSPITAL   (Germany)

^j UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

^k UNIVERSITY OF TÜBINGEN   (Germany)

^l TIMONE HOSPITAL   (France)

^m CHU PURPAN   (France)

ⁿ GUY S HOSPITAL   (United Kingdom)

^o KING'S COLLEGE LONDON   (United Kingdom)

^p Centre Hospitalo Universitaire Dr Benbadis Constantine   (Algeria)

^q Institut Pasteur d'Algerie   (Algeria)

^r HOSPITAL EGAS MONIZ   (Portugal)

^s HOSPITAL DO DIVINO ESPÍRITO SANTO   (Portugal)

^t UNIVERSITY OF PORTO   (Portugal)

^u HOSPITAL MARIA PIA   (Portugal)

^v Hospital So Sebastio   (Portugal)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA FETOPROTEIN; RNA HELICASE; SENATAXIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; APRAXIA; ARTICLE; ATAXIA OCULAR APRAXIA 2; AUTOSOMAL RECESSIVE DISORDER; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; CLINICAL FEATURE; FAMILY; GENE MUTATION; HUMAN; NONHUMAN; NUCLEOTIDE SEQUENCE; ONSET AGE; PRIORITY JOURNAL; RNA TRANSLATION; SCHOOL CHILD; SENSORIMOTOR NEUROPATHY;

ALPHA-FETOPROTEINS; CEREBELLAR ATAXIA; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; FUNGAL PROTEINS; HUMANS; MUTATION; OCULAR MOTILITY DISORDERS; RNA HELICASES; SACCHAROMYCES CEREVISIAE PROTEINS;

ATAXIA;

EID: 10744230604     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1303     Document Type: Article

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