A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures is a research paper published in Human Molecular Genetics (2021). On theSindex it has a DataRank of 0. It has been cited 16 times.
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Medical Research Council
Grant: 217065/Z/19/Z
Wellcome Trust
Grant: 082036/B/07/Z
University of Kansas
Grant: NIH:NIDCD 5 R01 DC001803
The Waterloo Foundation
Grant: 797–1720
Action Medical Research Action/The Chief Scientist Office (CSO), Scotland grant
Grant: GN2614
National Institutes of Health
Grant: 2R01DC001803-20
Morphosyntactic Abilities of SLI Probands
Wellcome Trust
Grant: 082036
Developmental relationships between dyslexia and specific languate impairment
Wellcome Trust
Grant: 105621
Institutional Strategic Support Fund Phase2 FY2014/16
Wellcome Trust
Grant: 217065
The Avon Longitudinal Study of Parents and Children (ALSPAC): A multi-generation, longitudinal resource focusing on life course health and well-being.
UK Research and Innovation
Grant: G1000569/1
Investigation of the roles of CMIP and ATP2C2 in Specific Language Impairment (SLI).
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Sustainable Development Goals