A BanI RFLP at a deletion hotspot in the human dystrophin gene.
作者信息
Read A P, Mountford R
机构信息
Department of Medical Genetics, St Mary's Hospital, Manchester, UK.
出版信息
Nucleic Acids Res. 1990 Jan 25;18(2):385. doi: 10.1093/nar/18.2.385.
Abstract
摘要
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本文引用的文献
1
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.对导致杜氏和贝克肌营养不良症的基因缺失的进一步研究。
Genomics. 1988 Feb;2(2):109-14. doi: 10.1016/0888-7543(88)90091-2.
2
Patterns of exon deletions in Duchenne and Becker muscular dystrophy.杜兴氏和贝克氏肌营养不良症中外显子缺失模式
Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859.
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