The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference22 articles.
1. Effect of Physical Exercise on Some Enzymes in the Serum
2. Serum levels of ATP: Creatine phosphotransferase (creatine kinase). The normal range and effect of muscular activity
3. Sources of error in the biochemical diagnosis of muscular dystrophy
4. THE VALUE OF SERUM ENZYME DETERMINATIONS IN THE IDENTIFICATION OF DYSTROPHIC CARRIERS
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1. Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology;Medical Hypotheses;2015-12
2. The manifesting carrier in Duchenne muscular dystrophy;Clinical Genetics;2008-04-23
3. Calf hypertrophy and asymmetry in female carriers of X-linked Duchenne muscular dystrophy: an over-diagnosed clinical manifestation;Clinical Genetics;2008-04-23
4. Recent Advances in Duchenne and Becker Muscular Dystrophy;Neurologic Clinics;1988-08
5. Identifying and circumventing the defect in Duchenne muscular dystrophy: Clinical and biochemical restoration after practical intervention;Medical Hypotheses;1987-10
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