Bi-Allelic Loss Of Function Variants In Slc30a5 As Cause Of Perinatal Lethal Cardiomyopathy (Dec, 10.1038/S41431-020-00803-8, 2020)

EUROPEAN JOURNAL OF HUMAN GENETICS(2021)

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Cardiovascular diseases,Development,Medical genetics,Medical genomics,Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics
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