A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome-Reference-Cited by-同舟云学术

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A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome

Published:2017 Issue:4 Volume:8 Page:211-218
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Baxter Adrianne L.,Vivian Jay L.,Hagelstrom R. Tanner,Hossain Waheeda,Golden Wendy L.,Wassman E. Robert,Vanzo Rena J.,Butler Merlin G.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mowat–Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions;International Journal of Molecular Sciences;2024-02-29

2. De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities;American Journal of Medical Genetics Part A;2023-09-25

3. “Liu-Liang-Chung” syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation;BMC Pediatrics;2023-09-21

4. Long-term selection on mitocoding genes buried in mammalian and avian nuclear genomes;2023-08-07

5. Mutated Transcripts of ZEB2 Do Not Undergo Nonsense-Mediated Decay in Mowat-Wilson Syndrome;Molecular Syndromology;2023

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