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Role of fibronectin mutations in spondylometaphyseal dysplasia and idiopathic scoliosis.

Role of fibronectin mutations in spondylometaphyseal dysplasia and idiopathic scoliosis.
纤连蛋白突变在脊柱干骺端发育不良和特发性脊柱侧凸中的作用。
批准号：
372375
负责人：
Campeau Philippe M
金额：
$49.6万
依托单位：
Centre hospitalier universitaire Sainte-Justine (Montral, Qubec)
依托单位国家：
加拿大
项目类别：
Operating Grants
财政年份：
2017
资助国家：
加拿大
项目状态：
已结题
起止时间：
2017-09-01 至 2022-09-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=372375&lang=en
关键词：
Fibronectin Scoliosis Skeletal Dysplasia

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中文摘要
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英文摘要
We identified rare mutations in the important matrix protein fibronectin in individuals with a rare bone disease affecting the spine and growth plates (spondylometaphyseal dysplasie) and in individuals with the common condition which is isolated scoliosis
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