Novel frameshift mutation in Indian autistic population causes neuroligin and neurexin binding defect
| Autor: | Hegde, Rajat, Hegde, Smita, Kulkarni, Suyamindra S., Pandurangi, Aditya, Gai, Pramod B., Das, Kusal K. |
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| Zdroj: | In Gene Reports September 2021 24 |
| Databáze: | ScienceDirect |
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