Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

Archives of Neurology

Volumn 60, Issue 4, 2003, Pages 610-614

  Alonso, Isabel ^a,b   Barros, José ^c   Tuna, Assunção ^c   Coelho, João ^a   Sequeiros, Jorge ^a,b   Silveira, Isabel ^a,b   Coutinho, Paula ^d  

^a UNIVERSITY OF PORTO   (Portugal)

^b UNIVERSITY OF PORTO   (Portugal)

^c HOSPITAL DE SANTO ANTÓNIO   (Portugal)

^d Hospital So Sebastio   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CALCIUM CHANNEL; GLUTAMINE;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; DOMINANT INHERITANCE; FAMILIAL HEMIPLEGIC MIGRAINE; FEMALE; GENETIC LINKAGE; HUMAN; LINKAGE ANALYSIS; MALE; MARKER GENE; MIGRAINE; MISSENSE MUTATION; PHENOTYPE; PORTUGAL; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; SPINOCEREBELLAR DEGENERATION; SPINOCEREBELLAR DEGENERATION TYPE 6;

ADOLESCENT; ADULT; ALANINE; CHILD; CYSTEINE; FEMALE; GLYCINE; HEMIPLEGIA; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MIGRAINE DISORDERS; MUTATION, MISSENSE; PHENOTYPE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SPINOCEREBELLAR ATAXIAS;

EID: 0344406276     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.60.4.610     Document Type: Article

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