A novel point mutation (G^<-1> to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy
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収録刊行物
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- Am J Hum Genet
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Am J Hum Genet 54 53-61, 1994
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- CRID
- 1573950399144873216
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- NII論文ID
- 10005659711
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- NII書誌ID
- AA00048454
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- データソース種別
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- CiNii Articles