Rad, A (2019) Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. American journal of human genetics.
Full text not available from this repository.| Item Type: | Article |
|---|---|
| Subjects: | R Medicine > R Medicine (General) |
| Depositing User: | Saeed Shoja |
| Date Deposited: | 23 Dec 2019 10:35 |
| Last Modified: | 23 Dec 2019 10:35 |
| URI: | http://eprints.medsab.ac.ir/id/eprint/1340 |
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