Published in

Wiley, Clinical Genetics, 5(90), p. 472-474, 2016

DOI: 10.1111/cge.12805

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DNM1L ‐related encephalopathy in infancy with Leigh syndrome‐like phenotype and suppression‐burst

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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