Absence of Family History and Phenotype–Genotype Correlation in Pediatric Brugada Syndrome: More Burden to Bear in Clinical and Genetic Diagnosis
Crossref DOI link: https://doi.org/10.1007/s00246-015-1133-5
Published Online: 2015-03-11
Published Print: 2015-06
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Daimi, Houria
Khelil, Amel Haj
Hamda, Khaldoun Ben
Aranega, Amelia
Chibani, Jemni B. E.
Franco, Diego
Text and Data Mining valid from 2015-03-11