CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum. (2021)
Attributed to:
Developing diagnostic methods for clinical genetics - phenotyping from faces in photos.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/cge.14022
PubMed Identifier: 34212383
Publication URI: http://europepmc.org/abstract/MED/34212383
Type: Journal Article/Review
Volume: 100
Parent Publication: Clinical genetics
Issue: 4
ISSN: 0009-9163