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Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

 

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Jun 2022969032
Jul 2022878612
Aug 2022858415
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Oct 202265558
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Jan 2023878316
Feb 2023837411
Mar 2023454512
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May 2023453616
Jun 2023514311
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Aug 2023504119
Sep 2023666513
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Nov 202321821311
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Jan 2024140134
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Mar 2024251167
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