Paediatric and adult ataxias (update 5)

European Journal of Paediatric Neurology

Volumn 10, Issue 5-6, 2006, Pages 249-253

  Morrison, Patrick J ^a  

^a ROYAL GROUP OF HOSPITALS TRUST   (United Kingdom)

Author keywords

Gene table movement disorders

Indexed keywords

ATAXIN 1; ATAXIN 3; ATAXIN 7; ATM PROTEIN; FRATAXIN; GENE PRODUCT; SPECTRIN;

ABETALIPOPROTEINEMIA; ADULT; ARTICLE; ATAXIA; ATAXIA TELANGIECTASIA; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CEREBELLAR ATAXIA; CHILD; CHROMOSOME 10P; CHROMOSOME 10Q; CHROMOSOME 11P; CHROMOSOME 11Q; CHROMOSOME 12P; CHROMOSOME 12Q; CHROMOSOME 13Q; CHROMOSOME 14Q; CHROMOSOME 15Q; CHROMOSOME 16P; CHROMOSOME 16Q; CHROMOSOME 18P; CHROMOSOME 19P; CHROMOSOME 19Q; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME 20P; CHROMOSOME 20Q; CHROMOSOME 22Q; CHROMOSOME 2P; CHROMOSOME 3P; CHROMOSOME 3Q; CHROMOSOME 4Q; CHROMOSOME 5Q; CHROMOSOME 6P; CHROMOSOME 6Q; CHROMOSOME 7Q; CHROMOSOME 8Q; CHROMOSOME 9P; CHROMOSOME 9Q; CHROMOSOME XQ; CONGENITAL DISORDER OF GLYCOSYLATION; FRIEDREICH ATAXIA; GENE LOCATION; GLOBOID CELL LEUKODYSTROPHY; HEREDITARY ATAXIA; HUMAN; METACHROMATIC LEUKODYSTROPHY; PRIORITY JOURNAL; REFSUM DISEASE; SENSORY NEUROPATHY; SPINOCEREBELLAR DEGENERATION; TAY SACHS DISEASE; WILSON DISEASE;

ADULT; ATAXIA; CHILD; CHILD, PRESCHOOL; HUMANS; PEDIATRICS;

EID: 33751307661     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2006.08.007     Document Type: Article

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