Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Open Access
- 30 May 2021
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 23 (9), 1715-1725
- https://doi.org/10.1038/s41436-021-01196-9
Abstract
No abstract availableKeywords
Funding Information
- Deutsche Forschungsgemeinschaft (RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1, RE 1723/5-1)
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