Kennedy disease by genetic analysis: one case report

doi:10.3877/cma.j.issn.2095-123X.2017.01.012

Chinese Journal of Brain Diseases and Rehabilitation(Electronic Edition) ›› 2017, Vol. 07 ›› Issue (01): 47-48. doi: 10.3877/cma.j.issn.2095-123X.2017.01.012

Special Issue: ；；；

• Case Report • Previous Articles

Kennedy disease by genetic analysis: one case report

Chunguang Li¹, Huanmin Li²()

Received:2016-08-18 Online:2017-02-01 Published:2017-02-01
Contact: Huanmin Li

Abstract

Chunguang Li, Huanmin Li. Kennedy disease by genetic analysis: one case report[J]. Chinese Journal of Brain Diseases and Rehabilitation(Electronic Edition), 2017, 07(01): 47-48.

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References 11

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[7]	鲁明，张俊，郑菊阳，等. 12例肯尼迪病患者肌电图和神经电图特点[J]．中国神经免疫学和神经病学杂志，2008, 15(3)：187-189.
[8]	Burgunder JM,Schôis L,Baets J, et al. EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders[J]. Eur J Neurol, 2011, 18(2)：207-217.
[9]	Atsuta N,Watanabe H,Ito M, et al. Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients[J]. Brain, 2006，129(6)：1446-1455.
[10]	鲁明，樊东升，宋红松，等. 亮丙瑞林治疗肯尼迪病的开放式研究[J]．中华神经科杂志，2013, 46(8): 544-545.
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