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A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation

Mendelian DisorderGenetic DisorderPqbp1 GeneGeneticsX-linked Mental RetardationPsychiatric GeneticsFragile X SpectrumMolecular BiologyTunisian FamilyMolecular GeneticsDisease Gene IdentificationGenomicsMedicineDevelopmental Delay