Guest guest Posted January 18, 2006 Report Share Posted January 18, 2006 Beijing Da Xue Xue Bao. 2006 Feb 18;38(1):78-9. Links No mutation was detected in the LMNA gene among sporadic Charcot- Marie-Tooth patients. Song SJ, Zhang YZ, Chen B, Wang MJ, Wang YY, Zhang YJ, Yan M, Zhong N. Peking University Center of Medical Genetics; Department of Medical Genetics, School of Basic Medical Sciences, Peking University, Beijing 100083, China. OBJECTIVE:To intensively investigate sporadic CMT patients, we have analyzed the LMNA gene in this study in a series of 32 unrelated CMT patients. METHODS: Twelve exons of the LMNA gene were amplified from genetomic DNA. PCR products of each exon were analyzed by single strand conformational polymorphism (SSCP). RESULTS: No abnormal SSCP pattern, suggesting no mutation in our CMT patients, was detected. CONCLUSION: The CMT diseases resulted from the mutations of LMNA gene were rare. Quote Link to comment Share on other sites More sharing options...
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