Duchenne/Becker muscular dystrophy: Correlation of phenotype by electroretinography with sites of DMD mutations.

被引：0
|
作者：
Pillers, DM
Weleber, RG
机构：
[1] Oregon Hlth Sci Univ, Dept Med & Mol Genet, Oregon Child Hlth Res Ctr, Doernbecher Childrens Hosp,Casey Eye Inst, Portland, OR 97201 USA
[2] Oregon Hlth Sci Univ, Dept Pediat, Oregon Child Hlth Res Ctr, Doernbecher Childrens Hosp,Casey Eye Inst, Portland, OR 97201 USA
[3] Oregon Hlth Sci Univ, Dept Ophthalmol, Oregon Child Hlth Res Ctr, Doernbecher Childrens Hosp,Casey Eye Inst, Portland, OR 97201 USA
来源：
JOURNAL OF INVESTIGATIVE MEDICINE | 1998年 / 46卷 / 01期
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：86A / 86A
页数：1
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