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1 article related to "Iddca"

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Articles

Case Report

Published on 13 May 2020

Severe Phenotype in a Patient With Homozygous 15q21.2 Microdeletion Involving BCL2L10, GNB5, and MYO5C Genes, Resembling Infantile Developmental Disorder With Cardiac Arrhythmias (IDDCA)

in Genetics of Common and Rare Diseases

Francesca L. Sciacca
Claudia Ciaccio
Federica Fontana
Camilla Strano
Francesca Gilardoni
Chiara Pantaleoni
Stefano D’Arrigo

Frontiers in Genetics

doi 10.3389/fgene.2020.00399

5,317 views
10 citations