Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features. (2020)

First Author: Scala M

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