Case report of a juvenile patient with autism spectrum disorder with a novel vombination of vopy number variants in ADGRL3 (LPHN3) and two pseudogenes
To our knowledge, this is the first report of a copy number variant in the ADGRL3 gene, and its first association with autism spectrum disorder in humans.
Gespeichert in:
| Hauptverfasser: | , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2 September 2022
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| In: |
The application of clinical genetics
Year: 2022, Jahrgang: 15, Pages: 125-131 |
| ISSN: | 1178-704X |
| DOI: | 10.2147/TACG.S361239 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.2147/TACG.S361239 Verlag, lizenzpflichtig, Volltext: https://www.dovepress.com/case-report-of-a-juvenile-patient-with-autism-spectrum-disorder-with-a-peer-reviewed-fulltext-article-TACG 
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| Verfasserangaben: | Martin H. Maurer, Anja Kohler, Melanie Hudemann, Jerome Jüngling, Saskia Biskup, Martin Menzel |
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