Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patients
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference34 articles.
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2. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy;Harley;Nature,1992
3. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy;Buxton;Nature,1992
4. Cloning of the essential myotonic dystrophy region and mapping of the putative defect;Aslanidis;Nature,1992
5. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
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