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A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family

19 Oct 2016

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PMID: 27871432
DOI: 10.1016/j.jns.2016.10.027

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A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi familyPMID 27871432Read ↗

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