Novel mutations in the Na+,K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

Annals of Neurology

Volumn 54, Issue 3, 2003, Pages 360-366

  Vanmolkot, Kaate R J ^a   Kors, Esther E ^a   Hottenga, Jouke Jan ^a   Terwindt, Gisela M ^a   Haan, Joost ^a,b   Hoefnagels, Wil A J ^c   Black, David F ^d   Sandkuijl, Lodewijk A ^a   Frants, Rune R ^a   Ferrari, Michel D ^a   Van den Maagdenberg, Arn M J M ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RIJNLAND HOSPITAL   (Netherlands)

^c De Honte Hospital   (Netherlands)

^d MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL P TYPE; CALCIUM CHANNEL Q TYPE;

ADULT; AGED; ARTICLE; ATP1A2 GENE; AUTOSOMAL DOMINANT DISORDER; BENIGN FAMILIAL INFANTILE CONVULSION; CACNA1A GENE; CHROMOSOME 19P; CHROMOSOME 1Q; CLINICAL ARTICLE; EPILEPSY; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY; FEMALE; GENE; GENE MUTATION; HAPLOTYPE; HUMAN; HUMAN CELL; ION TRANSPORT; MALE; MIGRAINE; MIGRAINE WITH AURA; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NETHERLANDS; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SEGREGATION ANALYSIS; SODIUM POTASSIUM ATPASE PUMP GENE;

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; ANIMALS; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; EPILEPSY, BENIGN NEONATAL; FEMALE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; MICE; MIDDLE AGED; MIGRAINE WITH AURA; MUTATION, MISSENSE; NA(+)-K(+)-EXCHANGING ATPASE; PEDIGREE; POLYMERASE CHAIN REACTION; RATS; SPECIES SPECIFICITY;

EID: 0041835844     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10674     Document Type: Article

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