An investigation of the carrier state in the Duchenne type muscular dystrophy.
作者信息
LEYBURN P, THOMSON W H, WALTON J N
出版信息
Ann Hum Genet. 1961 May;25:41-9. doi: 10.1111/j.1469-1809.1961.tb01495.x.
Abstract
摘要
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An investigation of the carrier state in the Duchenne type muscular dystrophy.
Ann Hum Genet. 1961 May;25:41-9. doi: 10.1111/j.1469-1809.1961.tb01495.x.
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引用本文的文献
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Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination.
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Serum aldolase and phosphocreatine kinase in umbilical cord blood.
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Serum enzymes in carriers of muscular dystrophy.
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CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY.
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SERUM ENZYME STUDIES IN MUSCLE DISEASE. III. SERUM CREATINE KINASE ACTIVITY IN RELATIVES OF PATIENTS WITH THE DUCHENNE TYPE OF MUSCULAR DYSTROPHY.
J Neurol Neurosurg Psychiatry. 1964 Jun;27(3):181-5. doi: 10.1136/jnnp.27.3.181.
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Sources of error in the biochemical diagnosis of muscular dystrophy.
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Aldolase activity in the plasma or serum of normal children and families with muscular dystrophy.
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A trial of therapy by nucleosides and nucleotides in muscular dystrophy.
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Alpha-hydroxybutyrate dehydrogenase activity in sex-linked muscular dystrophy.
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[Progressive muscular dystrophy. VII. Detection of heterozygotes of Duehenne muscular dystrophy by determining serum creatine kinase with localized work load in anoxia].
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