摘要篇首： Xp21 contiguous gene deletion syndrome, sometimes called complex glycerol kinase deficiency, is associated with variable size Xp21 deletions that usually include the glycerol kinase gene and span multiple Xp21 disease gene loci in the region. The order of the potentially affected loci are as follows:
作者单位Genetics Laboratory,Second Clinical College, China Medical University, Shenyang 110004, China[1]Department of Pediatrics,Second Clinical College, China Medical University, Shenyang 110004, China[2]Department of Radiology,Second Clinical College, China Medical University, Shenyang 110004, China[3]Genetics Laboratory, International Medical Research Center, Kobe University, Kobe 650-0017, Japan[4]
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