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

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Description scientific article
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author: Simon J McGowan  Nils Koelling  Katherine L Helbig  Han G. Brunner  Margot R F Reijnders  Eduardo Calpena  Christoffer Nellåker  Sarina G. Kant  Stephen Twigg  Andrew Oliver Mungo Wilkie 

Publication date May 31, 2018
Language English
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