中央轴空病的临床、遗传学及发病机制研究进展
被引量：1
摘要
中央轴空病（CCD）是一种先天性肌病，特征性的病理改变是I型肌纤维在氧化酶染色下出现中央轴空损害。近年来，随着临床病例报道的增多和分子生物学等技术的应用，对CCD的临床、分子遗传学及发病机制有了许多新的认识，现综述如下。
出处
《临床神经病学杂志》
CAS
北大核心
2011年第4期318-319,共2页
Journal of Clinical Neurology
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