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Elsevier (Cell Press), American Journal of Human Genetics, 5(70), p. 1368-1375, 2002

DOI: 10.1086/340390

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Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, with Myotonic Myopathy and Chondrodysplasia

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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