Servicio
Genética
Publicaciones (3) Publicaciones en las que ha participado algún/a investigador/a
2015
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A Genetically Vulnerable Myocardium May Predispose to Myocarditis
Journal of the American College of Cardiology
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Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1
Cerebellum
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Erratum: Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant (Seizure (2015) 25 (65-67))
Seizure