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Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder. (2024)

First Author: María Del Rocío PB

Attributed to: Resolving the basis of phenotypically variable hereditary abnormalities of eye formation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2024.08.07.24311381

PubMed Identifier: 39148819

Publication URI: http://europepmc.org/abstract/MED/39148819

Type: Journal Article/Review

Parent Publication: medRxiv : the preprint server for health sciences