– New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis
– International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework
– CNKSR2-related neurodevelopmental and epilepsy disorder: a cohort of 13 new families and literature review indicating a predominance of loss of function pathogenic variants
Polimorfismos, variantes, mutaciones: migraña, cardiomiopatía, epilepsia
Filed under Cardiopatías, Diagnóstico, Neurogenética, Neurología, Polimorfismos by on . 
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