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Mutation of KCC3: Understanding a sensory motor neuropathy

Mutation of KCC3: Understanding a sensory motor neuropathy
KCC3 突变:了解感觉运动神经病
批准号:
186342
负责人:
Rouleau Guy A
金额:
$31.11万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2009
资助国家:
加拿大
项目状态:
已结题
起止时间:
2009-03-01 至 2014-03-01

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中文摘要
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英文摘要
Hereditary motor and sensory neuropathy with agenesis of the corpus callosum (HMSN/ACC) is a severe and progressive hereditary disease that affects the brain and spinal cord. The main features of the disease include malformation of the bridge connecting t
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