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Cell Press, American Journal of Human Genetics, 6(60), p. 1535-1539, 1997

DOI: 10.1016/s0002-9297(07)64247-5

Cell Press, American Journal of Human Genetics, 6(60), p. 1535-1538

DOI: 10.1086/523989

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Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome.

This paper is available in a repository.
This paper is available in a repository.

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