Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features. (2020)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41431-020-0669-x
PubMed Identifier: 32572202
Publication URI: http://europepmc.org/abstract/MED/32572202
Type: Journal Article/Review
Volume: 28
Parent Publication: European journal of human genetics : EJHG
Issue: 11
ISSN: 1018-4813