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Variants identified in PTK7 associated with neural tube defects
BACKGROUND: Variants in planar cell polarity (PCP) pathway genes have been repeatedly implicated in the pathogenesis of NTDs in both mouse models and in human cohorts. Mouse models indicate that the homogenous disruption of the Ptk7 gene, a PCP regulator, results in craniorachischisis; while embryos...
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| 發表在: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2019
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6465732/ https://ncbi.nlm.nih.gov/pubmed/30689296 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.584 |
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