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Molecular Case Studies, 6(5), p. a003491, 2019

DOI: 10.1101/mcs.a003491

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Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

Journal article published in 2019 by J. Nicholas Cochran ORCID, Emily C. McKinley ORCID, Meagan Cochran, Michelle D. Amaral, Bryan A. Moyers, Brittany N. Lasseigne ORCID, David E. Gray, James M. J. Lawlor ORCID, Jeremy W. Prokop ORCID, Ethan G. Geier, James M. Holt ORCID, Michelle L. Thompson, J. Scott Newberry, Jennifer S. Yokoyama, Elizabeth A. Worthey and other authors.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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