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Resolving complex outcomes in 15q13.3 copy number variants using emerging diagnostic and biomarker tools

Resolving complex outcomes in 15q13.3 copy number variants using emerging diagnostic and biomarker tools
使用新兴诊断和生物标志物工具解决 15q13.3 拷贝数变异的复杂结果
批准号:
467360
负责人:
Singh Karun
金额:
$32.78万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2022
资助国家:
加拿大
项目状态:
未结题
起止时间:
2022-06-01 至 2025-06-01

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中文摘要
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英文摘要
Genetic changes affecting the copy number of chromosome 15q13.3 have been linked to a group of rare neurodevelopmental conditions including developmental delay, intellectual disability, autism spectrum disorder, epilepsy, schizophrenia, and others. The cr
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Investigating protein homeostasis and neurodevelopmental deficits in a recurrent microdeletion disorder
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海外基金