相似文献
1
X-linked dystrophies: from gene localization to gene therapy.
Curr Opin Neurol Neurosurg. 1992 Oct;5(5):610-4.
2
Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
Am J Med Genet. 1989 Feb;32(2):268-73. doi: 10.1002/ajmg.1320320231.
3
Update: Duchenne muscular dystrophy.
Compr Ther. 1988 Jul;14(7):29-32.
4
[New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
Z Arztl Fortbild (Jena). 1988;82(22):1139-42.
5
The new genetics and its application in the study of childhood muscular dystrophies.
J Assoc Physicians India. 1991 Dec;39(12):943-8.
6
[Linkage studies in Emery-Dreifuss muscular dystrophy].
J Genet Hum. 1989 Jun;37(2):127-32.
7
[Uses of RFLP analysis in detecting Duchenne muscular dystrophy gene carrier].
Zhonghua Yi Xue Za Zhi. 1991 Jun;71(6):339-41.
8
Duchenne muscular dystrophy in a girl identified by dystrophin deficiency.
Neuropediatrics. 1991 Aug;22(3):163-5. doi: 10.1055/s-2008-1071435.
9
Molecular biology of Duchenne and Becker's muscular dystrophy: clinical applications.
Ann Neurol. 1989 Aug;26(2):189-94. doi: 10.1002/ana.410260202.
10
Update on the molecular genetics of Duchenne muscular dystrophy.
Aust Paediatr J. 1988;24 Suppl 1:9-14.
引用本文的文献
1
Systemic gene transfer reveals distinctive muscle transduction profile of tyrosine mutant AAV-1, -6, and -9 in neonatal dogs.
Mol Ther Methods Clin Dev. 2014 Mar 5;1:14002. doi: 10.1038/mtm.2014.2.
Zotero 插件