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Springer Nature [academic journals on nature.com], European Journal of Human Genetics, 6(28), p. 763-769, 2020

DOI: 10.1038/s41431-020-0600-5

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De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability

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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