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Published on: September 16, 2019
[Gene diagnosis of facioscapulohumeral muscular dystrophy]
1Department of Neurology, Sun Yat-sen University of Medical Sciences, Guangzhou, Guangdong 510080 P. R. China. drzengying@21cn.com
Objective:
Perform gene diagnosis for Chinese facioscapulohumeral muscular dystrophy(FSHD).
Methods:
Digest genome DNA with restriction enzymes EcoR I only and EcoR I associated with Bln I. Use 0.6% agarose gel electrophoresis and Southern blotting hybridization with probe P13E11.
Results:
For FSHD patients, the sizes of EcoR I + Bln I/P13E11 DNA fragments ranged from 15kb to 33kb. For normal controls, they were over 41kb. Two presymptomatic patients were found.
Conclusion:
It is feasible to perform gene diagnosis and presymptomatic diagnosis for most Chinese FSHD patients by Southern blotting hybridization with probe P13E11, following double digestion of genome DNA with restriction enzymes EcoR I and Bln I.
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