Mutation rate in Duchenne type of muscular dystrophy.
作者信息
Gardner-Medwin D
出版信息
J Med Genet. 1970 Dec;7(4):334-7. doi: 10.1136/jmg.7.4.334.
Abstract
摘要
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Mutation rate in Duchenne type of muscular dystrophy.杜兴氏型肌营养不良症的突变率
J Med Genet. 1970 Dec;7(4):334-7. doi: 10.1136/jmg.7.4.334.
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Female carriers of Duchenne muscular dystrophy: a dilemma.
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Serum alpha-galactosidase activity in children with Duchenne-type muscular dystrophy and in gene carriers.杜氏型肌营养不良患儿及基因携带者的血清α-半乳糖苷酶活性
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Aminoglycoside-induced mutation suppression (stop codon readthrough) as a therapeutic strategy for Duchenne muscular dystrophy.氨基糖苷类诱导的突变抑制（终止密码子通读）作为杜氏肌营养不良症的一种治疗策略。
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A genetic study of Duchenne muscular dystrophy in West Midlands.西米德兰兹郡杜兴氏肌肉营养不良症的基因研究。
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Incidence of Duchenne muscular dystrophy in New South Wales and Australian Capital Territory.新南威尔士州和澳大利亚首都地区杜兴氏肌营养不良症的发病率。
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Epidemiology of Duchenne muscular dystrophy in the province of Turin.
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The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.杜氏肌营养不良孤立病例母亲的基因状况。
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The female carrier of Duchenne muscular dystrophy.杜氏肌营养不良症的女性携带者。
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[Monozygotic twins with progressive muscular dystrophy].
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本文引用的文献
1
Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds.肌肉疾病研究。五、33个家族中儿童进行性肌营养不良的遗传情况。
Am J Hum Genet. 1951 Jun;3(2):111-25.
2
Formal genetics of muscular dystrophy.肌营养不良症的形式遗传学
Am J Hum Genet. 1959 Dec;11(4):360-79.
3
Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.儿童期肌营养不良；遗传学方面；利兹地区临床类型及其遗传的实地研究。
Ann Hum Genet. 1959 Apr;23(2):127-63. doi: 10.1111/j.1469-1809.1958.tb01457.x.
4
Muscular dystrophy in Northern Ireland. IV. Some additional data.北爱尔兰的肌肉萎缩症。IV. 一些补充数据。
Ann Hum Genet. 1958 May;22(3):231-4. doi: 10.1111/j.1469-1809.1958.tb01417.x.
5
On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies.关于肌肉萎缩症的遗传；附带血型说明以及色觉与连锁研究说明。
Ann Hum Genet. 1955 Aug;20(1):1-38. doi: 10.1111/j.1469-1809.1955.tb01274.x.
6
Benign spinal muscular atrophy arising in childhood and adolescence.
J Neurol Sci. 1967 Jul-Aug;5(1):121-58. doi: 10.1016/0022-510x(67)90013-5.
7
The cardiomyopathy of progressive muscular dystrophy.进行性肌营养不良性心肌病
Circulation. 1966 Apr;33(4):625-48. doi: 10.1161/01.cir.33.4.625.
8
An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy.肌酸激酶检测在杜氏肌营养不良症携带者检测中的评估。
J Pediatr. 1967 Jul;71(1):82-93. doi: 10.1016/s0022-3476(67)80235-x.
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