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Molecular Psychiatry|March 31, 2022
Targeted therapy of cognitive deficits in fragile X syndromeA Puścian, M Winiarski, J Borowska, et al.
Clinical Genetics|September 22, 2018
Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spinesKrzysztof Szczałuba, Joanna J Chmielewska, Olga Sokolowska, et al.
HGG Advances|September 16, 2021
PTPN4 germline variants result in aberrant neurodevelopment and growthJoanna J Chmielewska, Deepika Burkardt, Jorge Luis Granadillo, et al.
Human Mutation|September 20, 2022
Destabilization of mutated human PUS3 protein causes intellectual disabilityTing-Yu Lin, Robert Smigiel, Bozena Kuzniewska, et al.
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