A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

MA Kaunisto; H Harno; KRJ Vanmolkot; JJ Gargus; G Sun; E Hämäläinen; E Liukkonen; M Kallela; AMJM van den Maagdenberg; RR Frants; M Färkkilä; A Palotie; M Wessman

doi:10.1007/s10048-004-0178-z

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

MA Kaunisto, H Harno, KRJ Vanmolkot, JJ Gargus, G Sun, E Hämäläinen, E Liukkonen, M Kallela, AMJM van den Maagdenberg, RR Frants, M Färkkilä, A Palotie, M Wessman

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

Originalspråk	engelska
Tidskrift	Neurogenetics
Volym	5
Utgåva	2
Sidor (från-till)	141-146
Antal sidor	6
ISSN	1364-6745
DOI	https://doi.org/10.1007/s10048-004-0178-z
Status	Publicerad - jun 2004
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Åtkomst av dokument

10.1007/s10048-004-0178-z

Citera det här

Kaunisto, MA., Harno, H., Vanmolkot, KRJ., Gargus, JJ., Sun, G., Hämäläinen, E., Liukkonen, E., Kallela, M., van den Maagdenberg, AMJM., Frants, RR., Färkkilä, M., Palotie, A., & Wessman, M. (2004). A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. Neurogenetics, 5(2), 141-146. https://doi.org/10.1007/s10048-004-0178-z

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title = "A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2",

keywords = "familial hemiplegic migraine, linkage, DNA sequence analysis, Na+-K+-exchanging ATPase, missense mutation, MASS-SPECTROMETRY, ALPHA-2 ISOFORM, DNA POOLS, NA,K-ATPASE, LOCUS, GENE, MAPS, MICE",

author = "MA Kaunisto and H Harno and KRJ Vanmolkot and JJ Gargus and G Sun and E H{\"a}m{\"a}l{\"a}inen and E Liukkonen and M Kallela and {van den Maagdenberg}, AMJM and RR Frants and M F{\"a}rkkil{\"a} and A Palotie and M Wessman",

year = "2004",

month = jun,

doi = "10.1007/s10048-004-0178-z",

language = "English",

volume = "5",

pages = "141--146",

journal = "Neurogenetics",

issn = "1364-6745",

publisher = "Springer",

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}

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. / Kaunisto, MA ; Harno, H; Vanmolkot, KRJ; Gargus, JJ; Sun, G; Hämäläinen, E; Liukkonen, E; Kallela, M; van den Maagdenberg, AMJM; Frants, RR; Färkkilä, M ; Palotie, A ; Wessman, M.

I: Neurogenetics, Vol. 5, Nr. 2, 06.2004, s. 141-146.

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

TY - JOUR

T1 - A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

AU - Kaunisto, MA

AU - Harno, H

AU - Vanmolkot, KRJ

AU - Gargus, JJ

AU - Sun, G

AU - Hämäläinen, E

AU - Liukkonen, E

AU - Kallela, M

AU - van den Maagdenberg, AMJM

AU - Frants, RR

AU - Färkkilä, M

AU - Palotie, A

AU - Wessman, M

PY - 2004/6

Y1 - 2004/6

KW - familial hemiplegic migraine

KW - linkage

KW - DNA sequence analysis

KW - Na+-K+-exchanging ATPase

KW - missense mutation

KW - MASS-SPECTROMETRY

KW - ALPHA-2 ISOFORM

KW - DNA POOLS

KW - NA,K-ATPASE

KW - LOCUS

KW - GENE

KW - MAPS

KW - MICE

U2 - 10.1007/s10048-004-0178-z

DO - 10.1007/s10048-004-0178-z

M3 - Article

VL - 5

SP - 141

EP - 146

JO - Neurogenetics

JF - Neurogenetics

SN - 1364-6745

IS - 2

ER -