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Keywords PRMT9 intellectual disability whole-exome sequencing primary cilium zebrafish neurodevelopmental disorder Introduction Affecting at least 1% of the population worldwide, intellectual disability is a major healthcare problem.1,2 Defined as a substantive limitation in intellectual functioning and adaptive behavior with an age of onset before 18 years, it is clinically and genetically highly heterogeneous.3 Sequencing efforts such as trio whole-exome sequencing (WES) or whole-genome...
Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request. Peer Review The peer review history for this article is available at https://www.webofscience.com/api/gateway/wos/peer-review/10.1111/cge.70041.
Conflicts of Interest The authors declare no conflicts of interest. Supporting Information Filename Description cge70041-sup-0001-TableS1.docxWord 2007 document , 14.9 KB Table S1: Primer sets used in the qPCR and qRT-PCR studies. References 1 and , “On the Classification, Natural History and Treatment of the Myopathies,” Brain: A Journal of Neurology 77, no. 2 (1954): 169–231, https://doi.org/10.1093/brain/77.2.169.
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