First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine

European Journal of Human Genetics

Volumn 15, Issue 8, 2007, Pages 884-888

  Vanmolkot, Kaate R J ^a   Stam, Anine H ^a   Raman, Ashok ^b   Koenderink, Jan B ^c   de Vries, Boukje ^a   van den Boogerd, Eelke H ^a   van Vark, Judith ^b   van den Heuvel, Jeroen J M W ^c   Bajaj, Nin ^b   Terwindt, Gisela M ^a   Haan, Joost ^a,d   Frants, Rune R ^a   Ferrari, Michel D ^a   van den Maagdenberg, Arn M J M ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b QUEEN S MEDICAL CENTRE   (United Kingdom)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d RIJNLAND HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM) 1A2; PROTEIN ATP1A2; UNCLASSIFIED DRUG;

ADULT; ALLELE; ARTICLE; CELL ASSAY; CELL SURVIVAL; CONFUSION; CONTROLLED STUDY; DISEASE DURATION; DISEASE SEVERITY; DISORIENTATION; DYSPHAGIA; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY; FEMALE; HEAD INJURY; HEADACHE; HEMIANOPIA; HEMIPLEGIA; HETEROZYGOSITY; HUMAN; HUMAN CELL; HYPEREMIA; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; MISSENSE MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOTOPHOBIA; PRIORITY JOURNAL; PROTEIN DEFECT; VOMITING;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CHILD; FEMALE; HETEROZYGOTE; HUMANS; MALE; MIGRAINE WITH AURA; MOLECULAR SEQUENCE DATA; NA(+)-K(+)-EXCHANGING ATPASE; PEDIGREE;

EID: 34547150579     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201841     Document Type: Article

References (14)

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