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Intragenic CNTNAP2 Deletions: A Bridge Too Far?
Intragenic deletions of the contactin-associated protein-like 2 gene (CNTNAP2) have been found in patients with Gilles de la Tourette syndrome, intellectual disability (ID), obsessive compulsive disorder, cortical dysplasia-focal epilepsy syndrome, autism, schizophrenia, Pitt-Hopkins syndrome, stutt...
Shranjeno v:
| izdano v: | Mol Syndromol |
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| Glavni avtor: | |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
S. Karger AG
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5448439/ https://ncbi.nlm.nih.gov/pubmed/28588433 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000456021 |
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