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Inherited Xp21 deletion in a boy with complex glycerol kinase deficiency syndrome |
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| Authors: | F. Saito J. Goto H. Kakinuma F. Nakamura S. Murayama I. Nakano A. Tonomura |
| Affiliation: | Department of Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University, 5–45 Yushimu I-chome, Bunkyo-ku, Tokyo, 113 Japan;Department of Neurology, Shimoshizu National Hospital and Sanatorium, Chiba;Department of Pediatrics, Shimoshizu National Hospital and Sanatorium, Chiba;Department of Neurology, Institute of Brain Research, Faculty of Medicine, University of Tokyo, Japan |
| Abstract: | |
| Keywords: | Adrenal hypoplasia glycerol kinase deficiency progressive muscular dystrophy Xp21 deletion |