<i>FOXG1</i>-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms

<i>FOXG1</i>-Related Syndrome: From Clinical to Molecular Genetics and Pathogenic Mechanisms

Individuals with mutations in forkhead box G1 (<i>FOXG1</i>) belong to a distinct clinical entity, termed &#8220;<i>FOXG1</i>-related encephalopathy&#8221;. There are two clinical phenotypes/syndromes identified in <i>FOXG1</i>-related encephalopathy, dupl...

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Bibliographic Details
Main Authors: Lee-Chin Wong, Shekhar Singh, Hsin-Pei Wang, Chia-Jui Hsu, Su-Ching Hu, Wang-Tso Lee
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:International Journal of Molecular Sciences
Subjects:
<i>FOXG1</i>
Rett syndrome
hyperkinetic movements
telencephalon
transcriptional factor
Online Access:https://www.mdpi.com/1422-0067/20/17/4176

Internet

https://www.mdpi.com/1422-0067/20/17/4176

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