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Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome (2021)

First Author: Wood K

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

Parent Publication: Clinical Genetics

Issue: 2

ISSN: 0009-9163