Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome (2022)

First Author: Wood Katherine

Attributed to: Investigating the emerging role of spliceosome mutations in craniofacial development disorders funded by MRC

No abstract provided

Type: Conference/Paper/Proceeding/Abstract

Volume: 30

Parent Publication: EUROPEAN JOURNAL OF HUMAN GENETICS

Issue: SUPPL 1

ISSN: 1018-4813