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2001 | 1 |
2004 | 1 |
2024 | 0 |
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Genomic organization and promoter analysis of human KCNN3 gene.
J Hum Genet. 2001;46(8):463-70. doi: 10.1007/s100380170046.
J Hum Genet. 2001.
PMID: 11501944
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
Kaunisto MA, Harno H, Vanmolkot KR, Gargus JJ, Sun G, Hämäläinen E, Liukkonen E, Kallela M, van den Maagdenberg AM, Frants RR, Färkkilä M, Palotie A, Wessman M.
Kaunisto MA, et al.
Neurogenetics. 2004 Jun;5(2):141-6. doi: 10.1007/s10048-004-0178-z. Epub 2004 May 7.
Neurogenetics. 2004.
PMID: 15133718
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