Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome. (2022)
Attributed to:
Understanding the role of U5 snRNP gene mutation in pre-messenger RNA splicing and craniofacial development
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/cge.14082
PubMed Identifier: 34713892
Publication URI: http://europepmc.org/abstract/MED/34713892
Type: Journal Article/Review
Volume: 101
Parent Publication: Clinical genetics
Issue: 2
ISSN: 0009-9163