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Elsevier, Genetics in Medicine, 9(23), p. 1715-1725, 2021

DOI: 10.1038/s41436-021-01196-9

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Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies

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

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