Identifying and understanding a new skeletal dysplasia caused by ERI1 mutations
Identifying and understanding a new skeletal dysplasia caused by ERI1 mutations
批准号:
472627
负责人:
Campeau Philippe M
金额:
$7.29万
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:
已结题
起止时间:
2022-09-01 至 2023-09-01
中文摘要
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英文摘要
Spondyloepimetaphyseal dysplasias (SEMD) comprise a genetically heterogeneous group of bone disorders characterized by developmental changes in the growth plates and vertebrae, and it leads to short stature, scoliosis and joint deformities often requiring
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