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Paper Details

Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.
Pediatr Neurol
5
2022
ID, PLXNA3, PLXNA3 cytoplasmic domain variants, PLXNA3 variant, PLXNA3 variants, Plexin, Plexin-A3, Semaphorin, Semaphorins, X chromosome, X-Linked Intellectual Disability Syndrome, X-linked intellectual disability syndrome, attention-deficit/hyperactivity traits, autism, boys, exons 22 to 32, fine motor dyspraxia, humans, intellectual disabilities, mice, neurodevelopmental disorder, neurodevelopmental disorders, patients, plexin, plexin gene, plexin receptor, plexin-A3, plexins, semaphorin

Datasets

Release 1.2