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Case Report—An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions.

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Title: Case Report—An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions.
Authors: Feichtinger, René G.1 (AUTHOR) r.feichtinger@salk.at, Preisel, Martin1 (AUTHOR) m.preisel@salk.at, Brugger, Karin1 (AUTHOR) kar.brugger@salk.at, Wortmann, Saskia B.1,2 (AUTHOR) h.mayr@salk.at, Mayr, Johannes A.1 (AUTHOR)
Source: Genes. Jun2023, Vol. 14 Issue 6, p1217. 9p.
Database: Academic Search Ultimate
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  Data: Case Report—An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions.
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      – TitleFull: Case Report—An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions.
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              Text: Jun2023
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              Y: 2023
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