Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome. (2021)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2021.04.016
PubMed Identifier: 33991472
Publication URI: http://europepmc.org/abstract/MED/33991472
Type: Journal Article/Review
Volume: 108
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297