Racial effect on serum creatine-kinase: Implications for estimation of heterozygosity risks for females at-risk for Duchenne dystrophy
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference22 articles.
1. Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: A Brazilian study;Zatz;J Genet Hum,1976
2. Serum creatine-kinase and pyruvate-kinase in Duchenne muscular dystrophy carrier detection;Percy;Muscle nerve,1979
3. Serum pyruvate-kinase (PK) and creatine-phophokinase (CPK) in females relatives and patients with X-linked muscular dystrophies (Duchenne and Becker);Zatz;J Neurol Sci,1980
4. Evaluation of carrier detection rates for Duchenne and Becker muscular dystrophies using serum creatinekinase (CK) and pyruvate-kinase (PK) through discrimination analysis;Zatz;Am J Med Genet,1986
5. Carrier detection in Duchenne muscular dystrophy: a review of current issues and approaches;Gruemer;Clin Chim Acta,1987
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1. Serum Muscle Enzymes in Neuromuscular Disease;Neuromuscular Disorders in Clinical Practice;2013-04-26
2. Clinical variability in calpainopathy: What makes the difference?;European Journal of Human Genetics;2002-12
3. Creatine Kinase Revisited;Journal of Clinical Neuromuscular Disease;2001-03
4. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G;American Journal of Medical Genetics;1999-02-19
5. Estimates of Genetic and Environmental Components of Serum Isocitrate Dehydrogenase (ICDH) in Normal Twins;Acta geneticae medicae et gemellologiae: twin research;1991-01
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