Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation

Neuromuscular Disorders

Volumn 17, Issue 11-12, 2007, Pages 968-969

  Nahas, S A ^a   Duquette, A ^b   Roddier, K ^b   Gatti, R A ^a   Brais, B ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CENTRE HOSPITALIER DE L UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

AOA2; Cancer risk; French Canadian; Ionizing radiation; Spinocerebellar ataxia

Indexed keywords

ARTICLE; ATAXIA; ATAXIA OCULOMOTOR APRAXIA 2; CANCER RISK; CELL ASSAY; CONTROLLED STUDY; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; IONIZING RADIATION; LYMPHOBLASTOID CELL LINE; MISSENSE MUTATION; PRIORITY JOURNAL; RADIOSENSITIVITY; SPINOCEREBELLAR DEGENERATION;

ADOLESCENT; ALPHA-FETOPROTEINS; APRAXIAS; ATAXIA; CELL LINE; CHILD; COLONY-FORMING UNITS ASSAY; DNA MUTATIONAL ANALYSIS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LYMPHOCYTES; MUTATION; NEOPLASMS; OCULAR MOTILITY DISORDERS; PROGNOSIS; QUEBEC; RADIATION, IONIZING; RNA HELICASES;

EID: 36348950459     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2007.06.464     Document Type: Article

References (5)

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5. Nemeth A.H., Bochukova E., Dunne E., et al. Autosomal-recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34. Am J Hum Genet 67 5 (2000) 1320-1326