Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/2/11/1877/2028621/2-11-1877.pdf
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