Missense CACNA1A mutation causing episodic ataxia type 2

Archives of Neurology

Volumn 58, Issue 2, 2001, Pages 292-295

  Denier, C ^a   Ducros, A ^a   Durr, A ^a   Eymard, B ^a   Chassande, B ^a   Tournier Lasserve, E ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; CASE REPORT; CASE STUDY; CHROMOSOME 19; CLINICAL FEATURE; DISEASE CLASSIFICATION; EPISODIC ATAXIA TYPE 2; EXON; GENOTYPE; HUMAN; MALE; MISSENSE MUTATION; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 0035115339     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.58.2.292     Document Type: Article

References (20)

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20. 2+ channels