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Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome (2021)

First Author: Pottie L

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

Parent Publication: The American Journal of Human Genetics

Issue: 6

ISSN: 0002-9297