Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy. (2020)
Attributed to:
Discovering the causes of mutation-negative hypertrophic cardiomyopathy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/cge.13759
PubMed Identifier: 32335906
Publication URI: http://europepmc.org/abstract/MED/32335906
Type: Journal Article/Review
Volume: 98
Parent Publication: Clinical genetics
Issue: 1
ISSN: 0009-9163