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Paper Details

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Molecular Psychiatry
5
2023
CAS, Childhood apraxia of speech, DDX3X, SETBP1, SETD1A, candidate genes, child speech disorder, childhood speech disorder, chromatin, genes, neurodevelopmental disorders, short tandem repeat variants, single genes, trio
Author NameAffiliation
Michael S HildebrandUniversity of Melbourne
Michael S HildebrandMurdoch Children's Research Institute
Mark F BennettThe Walter and Eliza Hall Institute of Medical Research
Mark F BennettUniversity of Melbourne
Ingrid E SchefferUniversity of Melbourne
Melanie BahloThe Walter and Eliza Hall Institute of Medical Research
Melanie BahloUniversity of Melbourne
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Release 1.2