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CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum. (2021)

First Author: Palmer EE

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