A novel silent mutation in the NSDHL gene causing CHILD syndrome as a result of aberrant splicing

被引:0
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作者
Saito, M [1 ]
Ishiko, A [1 ]
机构
[1] Keio Univ, Sch Med, Tokyo, Japan
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R75 [皮肤病学与性病学];
学科分类号
100206 ;
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450
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页码:A75 / A75
页数:1
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