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Springer Nature [academic journals on nature.com], European Journal of Human Genetics, 6(24), p. 949-953, 2015

DOI: 10.1038/ejhg.2015.217

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De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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