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Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies (2021)

First Author: Gabriel C. Dworschak

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.60692/9pg9j-vsv28

Publication URI: https://gresis.osc.int//doi/10.60692/9pg9j-vsv28

Type: Other