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POGZ de novo missense variants in neuropsychiatric disorders
BACKGROUND: De novo likely gene‐disrupting variants of POGZ cause autism spectrum disorder (ASD) and intellectual disability. However, de novo missense variants of this gene were not well explored in neuropsychiatric disorders. METHODS: The single‐molecule molecular inversion probes‐based targeted s...
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| I publikationen: | Mol Genet Genomic Med |
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| Huvudupphovsmän: | , , , , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
John Wiley and Sons Inc.
2019
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6732319/ https://ncbi.nlm.nih.gov/pubmed/31347273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.900 |
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