Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome (2022)
Attributed to:
Investigating the emerging role of spliceosome mutations in craniofacial development disorders
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Type: Conference/Paper/Proceeding/Abstract
Volume: 30
Parent Publication: EUROPEAN JOURNAL OF HUMAN GENETICS
Issue: SUPPL 1
ISSN: 1018-4813