Case report: A de novo variant of CRMP1 in an individual with a neurodevelopmental disorder
Currently, the <i>CRMP1</i> gene has no clear disease phenotype association in the Online Mendelian Inheritance in Man (OMIM) database. Our report may provide evidence for an association between the <i>CRMP1</i> gene and neurodevelopmental disorders (NDDs).
Authors
- Jia Chen (ORCID: https://orcid.org/0000-0002-1672-4607)
- Juan Liu (ORCID: https://orcid.org/0000-0003-1399-6719)
- Qi Wang (ORCID: https://orcid.org/0000-0002-1556-2167)
Institutions
- Chengdu Medical College (CN)
- Mianyang Central Hospital (CN)
Publication Details
- Journal
- Frontiers in Neuroscience
- Published
- 2024-12-20
- DOI
- https://doi.org/10.3389/fnins.2024.1490731
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00