De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

Reference

Reijnders, Margot R.F., et al. “De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder”. The American Journal of Human Genetics, vol. 102, no. 6, May 2018, pp. 1195–1203, https://doi.org/10.1016/j.ajhg.2018.04.014.

PubMed Reference Number (PMID)

29861108