Saisuda Noojarern on Muck Rack

Saisuda Noojarern

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Articles

A novel AP1S2 variant causing leaky splicing in X‐linked intellectual disability: Further delineation and intrafamilial variability

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By Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong
| pericles.pericles-prod.literatumonline.com
CONFLICT OF INTEREST STATEMENT The authors declare no conflicts of interest. Supporting Information Filename Description ajmga63639-sup-0001-Supinfo.pdfPDF document, 972.9 KB Appendix S1: Supporting information. REFERENCES , , , , , , , & (2012). Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia. European Journal of Medical Genetics, 55(2), 124–127. https://doi.org/10.1016/j.ejmg.2011.12.001 , , , , , , , , , , & (2008).
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A novel AP1S2 variant causing leaky splicing in X‐linked intellectual disability: Further delineation and intrafamilial variability

|
By Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong
| Wiley Online Library Verified
CONFLICT OF INTEREST STATEMENT The authors declare no conflicts of interest. Supporting Information Filename Description ajmga63639-sup-0001-Supinfo.pdfPDF document, 972.9 KB Appendix S1: Supporting information. REFERENCES , , , , , , , & (2012). Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia. European Journal of Medical Genetics, 55(2), 124–127. https://doi.org/10.1016/j.ejmg.2011.12.001 , , , , , , , , , , & (2008).
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