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Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
Eur J Hum Genet. 2015 Jan;23(1):79-85. doi: 10.1038/ejhg.2014.54. Epub 2014 Mar 26.
Eur J Hum Genet. 2015.
PMID: 24667783
Free PMC article.
Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p.
Gurrieri F, Zollino M, Oliva A, Pascali V, Orteschi D, Pietrobono R, Camporeale A, Coll Vidal M, Partemi S, Brugada R, Bellocci F, Neri G.
Gurrieri F, et al. Among authors: coll vidal m.
Eur J Hum Genet. 2013 Sep;21(9):965-9. doi: 10.1038/ejhg.2012.280. Epub 2013 Mar 20.
Eur J Hum Genet. 2013.
PMID: 23511928
Free PMC article.
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Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.
Parisi P, Oliva A, Coll Vidal M, Partemi S, Campuzano O, Iglesias A, Pisani D, Pascali VL, Paolino MC, Villa MP, Zara F, Tassinari CA, Striano P, Brugada R.
Parisi P, et al. Among authors: coll vidal m.
Epilepsy Res. 2013 Aug;105(3):415-8. doi: 10.1016/j.eplepsyres.2013.02.024. Epub 2013 Mar 25.
Epilepsy Res. 2013.
PMID: 23538271
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