Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.
作者信息
Laing N G, Akkari P A, Chandler D C, Thomas H E, Layton M G, Mears M E, Kakulas B A
机构信息
Australian Neuromuscular Research Institute, Queen Elizabeth II Medical Centre, Nedlands, Western Australia.
出版信息
Nucleic Acids Res. 1990 Jul 25;18(14):4284. doi: 10.1093/nar/18.14.4284.
Abstract
摘要
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Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.杜兴氏肌营养不良症（DMD）基因的互补脱氧核糖核酸（cDNA）8个PstI和TaqI多态性涉及HindIII图谱的第51外显子。
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引用本文的文献
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A TaqI map of the dystrophin gene useful for deletion and carrier status analysis.一种用于缺失和携带者状态分析的肌营养不良蛋白基因的TaqI图谱。
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本文引用的文献
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Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele.遗传性杜氏肌营养不良缺失等位基因的产前检测
Neurology. 1987 Feb;37(2):355-6. doi: 10.1212/wnl.37.2.355.
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RFLP for Duchenne muscular dystrophy cDNA clone 44-1.杜兴氏肌营养不良症cDNA克隆44-1的限制性片段长度多态性分析
Nucleic Acids Res. 1988 Jul 25;16(14B):7209. doi: 10.1093/nar/16.14.7209.
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