[杜兴氏型进行性肌营养不良携带者的生化、组织学和临床发现] - Suppr | 超能文献

[Biochemical, histological and clinical findings in carriers of Duchenne-type progressive muscular dystrophy].

作者信息

Moser H, Mumenthaler M, Wiesmann U

出版信息

Schweiz Med Wochenschr. 1971 Apr 17;101(15):537-42.

Abstract

摘要

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[Biochemical, histological and clinical findings in carriers of Duchenne-type progressive muscular dystrophy].[杜兴氏型进行性肌营养不良携带者的生化、组织学和临床发现]

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Carrier detection in X-linked muscular dystrophy.X连锁型肌营养不良的携带者检测

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Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.杜兴氏/贝克氏肌营养不良女性携带者血液中X染色体失活偏倚与血清肌酸激酶水平之间无相关性。

Am J Med Genet. 1998 Dec 4;80(4):356-61.

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[Present-day clinico-genetic framework of Duchenne's muscular dystrophy].

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Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian study.X连锁肌营养不良患者亲属的肌酸磷酸激酶（CPK）活性：一项巴西的研究。

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Comparative analysis between Duchenne and Becker types muscular dystrophy.杜兴氏和贝克氏型肌营养不良症的比较分析

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引用本文的文献

1

Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.杜氏肌营养不良症：发病机制及基因预防

Hum Genet. 1984;66(1):17-40. doi: 10.1007/BF00275183.

2

Muscle ribosomal protein synthesis in normal pregnancy: implication for carrier detection in Duchenne muscular dystrophy.正常妊娠期间肌肉核糖体蛋白合成：对杜氏肌营养不良症携带者检测的意义。

J Med Genet. 1974 Jun;11(2):114-6. doi: 10.1136/jmg.11.2.114.