Associated Papers
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay.
Ha T et al.
American Journal of Medical Genetics. Part A, 2024
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder.
Yahia A et al.
Human Genetics, 2024
Novel DIP2C gene splicing variant in an individual with focal infantile epilepsy.
Yang L et al.
American Journal of Medical Genetics. Part A, 2022
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