The neurobiology of Duchenne muscular dystrophy:: learning lessons from muscle?

被引:147
作者
Blake, DJ [1 ]
Kröger, S
机构
[1] Univ Oxford, Dept Human Anat & Genet, Oxford OX1 3QX, England
[2] Max Planck Inst Brain Res, Dept Neuroanat, D-60528 Frankfurt, Germany
基金
英国惠康基金;
关键词
D O I
10.1016/S0166-2236(99)01510-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several forms of inherited muscular dystrophy are associated with brain abnormalities and cognitive impairment. One of the most common and severe of these diseases is Duchenne muscular dystrophy (DMD), Dystrophin, the product of the DMD gene, is found in neurones, where it is associated with the postsynaptic membrane. Cognitive impairment in individuals with DMD is thought to be due to an abnormality in the neuronal membrane that is caused by lack of dystrophin, Recent experimental evidence has provided valuable clues in our understanding of the complex molecular neurobiology of muscular dystrophy.
引用
收藏
页码:92 / 99
页数:8
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