Genetics of congenital arrhythmia syndromes: the challenge of variant interpretation
Author:
Funder
NHGRI
National Institutes of Health
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
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4. ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering Variants;2023-09-08
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