De Novo and Inherited Loss-of-Function Variants in TLK2 :...

The American Journal of Human Genetics 2018 / 06 Vol. 102; Iss. 6

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

Reijnders, Margot R.F., Miller, Kerry A., Alvi, Mohsan, Goos, Jacqueline A.C., Lees, Melissa M., de Burca, Anna, Henderson, Alex, Kraus, Alison, Mikat, Barbara, de Vries, Bert B.A., Isidor, Bertrand,
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Volume:
102
Language:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2018.04.014
Date:
June, 2018
File:
PDF, 1.31 MB
english, 2018
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