Padberg G W
Department of Neurology, University Hospital Nijmegen, The Netherlands.
Curr Opin Neurol. 1993 Oct;6(5):688-94. doi: 10.1097/00019052-199310000-00003.
Recent progress in molecular genetics has resulted in more insight in the molecular biology of muscles and the muscular dystrophies, and has provided more reliable tools for prenatal and presymptomatic diagnosis in several disorders. The state of research is reviewed with emphasis on genetic aspects.
分子遗传学的最新进展使我们对肌肉及肌肉萎缩症的分子生物学有了更深入的了解，并为多种疾病的产前和症状前诊断提供了更可靠的工具。本文重点从遗传学方面对研究现状进行综述。
