Novel de novo mutations in EFTUD2 detected by exome sequencing in mandibulofacial dysostosis with Microcephaly syndrome
- PMID: 25735261
- DOI: 10.1002/ajmg.a.36948
Novel de novo mutations in EFTUD2 detected by exome sequencing in mandibulofacial dysostosis with Microcephaly syndrome
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources