Open Access UCL Research: SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups https://t.co/liMyUH3cTA
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RT @colleencaleshu: #CardioGen #HRS2019 Whew! That was A LOT of data on children with SCN5A disease. So much important information in here…
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RT @colleencaleshu: #CardioGen #HRS2019 Whew! That was A LOT of data on children with SCN5A disease. So much important information in here…
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RT @yanushidw: Identifying risk factors for cardiac events in #SCN5A positive children: a multicentre study across 13 countries by Alban Ba…