ZNF423 patient variants, truncations, and in-frame deletions in mice define an allele-dependent range of midline brain abnormalities

Author:

Deshpande OjasORCID,Lara Raquel Z.ORCID,Zhang Oliver R.ORCID,Concepcion Dorothy,Hamilton Bruce A.ORCID

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference58 articles.

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3. Analysis of protein-coding genetic variation in 60,706 humans;M Lek;Nature,2016

4. Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes;KJ Karczewski;bioRxiv,2019

5. Genome-wide genetic data on ~500,000 UK Biobank participants;C Bycroft;bioRxiv,2017

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