ENORMOUS DYSTROPHIN IN A PATIENT WITH BECKER MUSCULAR-DYSTROPHY

被引：31

作者：

ANGELINI, C ^{[1
]}

BEGGS, AH ^{[1
]}

HOFFMAN, EP ^{[1
]}

FANIN, M ^{[1
]}

KUNKEL, LM ^{[1
]}

机构：

[1] HARVARD UNIV, CHILDRENS HOSP,SCH MED,DEPT PEDIAT,DIV GENET, HOWARD HUGHES MED INST, BOSTON, MA 02115 USA

来源：

NEUROLOGY | 1990年 / 40卷 / 05期

关键词：

D O I：

10.1212/WNL.40.5.808

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：808 / 812

页数：5

共 19 条

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[6] FAMILIAL X-LINKED MYALGIA AND CRAMPS - A NONPROGRESSIVE MYOPATHY ASSOCIATED WITH A DELETION IN THE DYSTROPHIN GENE
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[7] IMPROVED DIAGNOSIS OF BECKER MUSCULAR-DYSTROPHY BY DYSTROPHIN TESTING
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[J]. NEUROLOGY, 1989, 39 (08) : 1011 - 1017
[8] DYSTROPHIN ABNORMALITIES IN DUCHENNE-BECKER MUSCULAR-DYSTROPHY
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[J]. NEURON, 1989, 2 (01) : 1019 - 1029
[9] CHARACTERIZATION OF DYSTROPHIN IN MUSCLE-BIOPSY SPECIMENS FROM PATIENTS WITH DUCHENNES OR BECKERS MUSCULAR-DYSTROPHY
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[10] CONSERVATION OF THE DUCHENNE MUSCULAR-DYSTROPHY GENE IN MICE AND HUMANS
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[J]. SCIENCE, 1987, 238 (4825) : 347 - 350

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