Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. (2022)

First Author: Khalaf-Nazzal R
Attributed to:  Precision Medicine Exeter Innovation Platform (PMEI Platform) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2022.09.012

PubMed Identifier: 36283405

Publication URI: http://europepmc.org/abstract/MED/36283405

Type: Journal Article/Review

Volume: 109

Parent Publication: American journal of human genetics

Issue: 11

ISSN: 0002-9297