Paediatric and adult recessive ataxias (update 6)

European Journal of Paediatric Neurology

Volumn 14, Issue 3, 2010, Pages 264-266

  Morrison, Patrick J ^a  

^a ROYAL GROUP OF HOSPITALS TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT;

ABETALIPOPROTEINEMIA; ADULT; ALPHA TOCOPHEROL DEFICIENCY; ARTICLE; ATAXIA NEURONAL MIGRATION; ATAXIA OCULOMOTOR APRAXIA; ATAXIA TELANGIECTASIA; ATAXIA TELANGIECTASIA LIKE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; CARBOHYDRATE DEFICIENCY; CAYMAN ISLAND ATAXIA; CEREBELLAR ATAXIA DEVELOPMENTAL DELAY; CHARLEVOIX SAGUENAY ATAXIA; CHILD; CHILDHOOD ONSET ATAXIA EPILEPSY; COENZYME Q10 DEFICIENCY 1; COENZYME Q10 DEFICIENCY 2; COENZYME Q10 DEFICIENCY 3; COENZYME Q10 DEFICIENCY 4; COENZYME Q10 DEFICIENCY LEIGH TYPE; CONGENITAL ATAXIA; EPILEPSY; FRAGILE X CEREBELLAR ATAXIA; FRIEDREICH ATAXIA; GENE LOCATION; GLOBOID CELL LEUKODYSTROPHY; GLYCOPROTEIN TYPE 1A DEFICIENCY; HEARING IMPAIRMENT; HUMAN; INFANT; INFANTILE ATAXIA; INFANTILE ONSET ATAXIA EPILEPSY; JOUBERT ATAXIA; KIDNEY TUBULE DISORDER; LEUKODYSTROPHY; METACHROMATIC ATAXIA; MYOCLONUS EPILEPSY; NEUROPATHY; POSTERIOR COLUMN ATAXIA; PRIORITY JOURNAL; REFSUM DISEASE I; REFSUM DISEASE II; REFSUM DISEASE III; RETINITIS; SENSORY NEUROPATHY; SIALIC ACID ATAXIA; SIDEROBLASTIC ANEMIA; SPINOCEREBELLAR ATAXIA 1; SPINOCEREBELLAR ATAXIA 2; SPINOCEREBELLAR ATAXIA 3; SPINOCEREBELLAR ATAXIA 4; SPINOCEREBELLAR ATAXIA 5; SPINOCEREBELLAR ATAXIA 6; SPINOCEREBELLAR ATAXIA 7; SPINOCEREBELLAR ATAXIA 8; SPINOCEREBELLAR ATAXIA 9; SPINOCEREBELLAR DEGENERATION; TAY SACHS DISEASE; UNVERRICHT LUNDBORG ATAXIA; WILSON DISEASE; X CHROMOSOME RECESSIVE INHERITANCE;

ADULT; CHILD; CHROMOSOMES; GENES; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INHERITANCE PATTERNS; MUTATION; NERVE TISSUE PROTEINS; SPINOCEREBELLAR DEGENERATIONS; STATISTICS AS TOPIC;

EID: 77950595326     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2009.10.001     Document Type: Article

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