Associated Papers
Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy.
Bainbridge MN et al.
Bmc Medical Genetics, 2017
28253841 (PubMed )
Supplement: 12881_2017_385_MOESM1_ESM.pdf
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
Pippucci T et al.
Plos One, 2013
24358150 (PubMed )
Supplement: pone.0082154.s002.xls › Sheet1
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