A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. (2021)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddab111
PubMed Identifier: 33864365
Publication URI: http://europepmc.org/abstract/MED/33864365
Type: Journal Article/Review
Volume: 30
Parent Publication: Human molecular genetics
Issue: 12
ISSN: 0964-6906