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.
Saved in:
| 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 |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!
