Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy (2022)

First Author: Lesurf R
Attributed to:  UK Infrastructure for Large-scale Clinical Genomics Research funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41525-022-00288-y

PubMed Identifier: 35288587

Publication URI: http://europepmc.org/abstract/MED/35288587

Type: Journal Article/Review

Parent Publication: npj Genomic Medicine

Issue: 1