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Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.
J Med Genet. 2004 Mar;41(3):e35. doi: 10.1136/jmg.2003.013938.
J Med Genet. 2004.
PMID: 14985406
Free PMC article.
No abstract available.
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity.
Malacarne M, Gennaro E, Madia F, Pozzi S, Vacca D, Barone B, dalla Bernardina B, Bianchi A, Bonanni P, De Marco P, Gambardella A, Giordano L, Lispi ML, Romeo A, Santorum E, Vanadia F, Vecchi M, Veggiotti P, Vigevano F, Viri F, Bricarelli FD, Zara F.
Malacarne M, et al.
Am J Hum Genet. 2001 Jun;68(6):1521-6. doi: 10.1086/320596. Epub 2001 Apr 20.
Am J Hum Genet. 2001.
PMID: 11326335
Free PMC article.
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