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FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family
BACKGROUND: Children with autism spectrum disorder (ASD) display impressive clinical heterogeneity, also involving treatment response. Genetic variants can contribute to explain this large interindividual phenotypic variability. METHODS: Array‐CGH (a‐CGH) and whole genome sequencing (WGS) were perfo...
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| Udgivet i: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley and Sons Inc.
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7507005/ https://ncbi.nlm.nih.gov/pubmed/32588496 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1373 |
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