Academic Journal
P207: Comprehensive phenotypic spectrum of MED13L syndrome: Insights from literature and the National Brain Gene Registry
| Title: | P207: Comprehensive phenotypic spectrum of MED13L syndrome: Insights from literature and the National Brain Gene Registry |
|---|---|
| Authors: | Muhammed Cagri Bayraktutan, Abigail Sveden, Sonal Mahida, Maya Chopra |
| Source: | Genetics in Medicine Open, Vol 3, Iss , Pp 102172- (2025) |
| Publisher Information: | Elsevier, 2025. |
| Publication Year: | 2025 |
| Collection: | LCC:Genetics LCC:Medicine |
| Subject Terms: | Genetics, QH426-470, Medicine |
| Document Type: | article |
| File Description: | electronic resource |
| Language: | English |
| ISSN: | 2949-7744 |
| Relation: | http://www.sciencedirect.com/science/article/pii/S2949774425002110; https://doaj.org/toc/2949-7744 |
| DOI: | 10.1016/j.gimo.2025.102172 |
| Access URL: | https://doaj.org/article/a7f14adf3a3b453a991a2393825f0e0c |
| Accession Number: | edsdoj.7f14adf3a3b453a991a2393825f0e0c |
| Database: | Directory of Open Access Journals |
| ISSN: | 29497744 |
|---|---|
| DOI: | 10.1016/j.gimo.2025.102172 |
| Published in: | Genetics in Medicine Open |
| Language: | English |