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GTF3C3 gene
Known as:
GTF3C3
, general transcription factor IIIC subunit 3
, General Transcription Factor IIIC, Polypeptide 3, 102kDa Gene
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This gene is involved in transcriptional regulation.
National Institutes of Health
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Related topics
Related topics
5 relations
GTF3C3 protein, human
Homo sapiens
Transcription, Genetic
Transcriptional Regulation
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study
S. Papuc
,
L. Abela
,
+28 authors
A. Rauch
European Journal of Human Genetics
2018
Corpus ID: 54633002
Early-onset epileptic encephalopathy (EE) and combined developmental and epileptic encephalopathies (DEE) are clinically and…
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2017
2017
Expanding the genetic heterogeneity of intellectual disability
S. Anazi
,
S. Maddirevula
,
+40 authors
F. Alkuraya
Human Genetics
2017
Corpus ID: 253970955
Intellectual disability (ID) is a common morbid condition with a wide range of etiologies. The list of monogenic forms of ID has…
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Review
2015
Review
2015
First Korean Case of SATB2-Associated 2q32-q33 Microdeletion Syndrome
Nae Yu
,
Saeam Shin
,
Kyung-A Lee
Annals of Laboratory Medicine
2015
Corpus ID: 9903099
Chromosome 2q32-q33 deletion syndrome (Online Mendelian Inheritance in Man [OMIM]*612313) is a chromosomal disorder that was…
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2011
2011
Modulation of chromatin modifying factors' gene expression in embryonic and induced pluripotent stem cells.
C. Luzzani
,
C. Solari
,
+7 authors
Alejandra S. Guberman
Biochemical and Biophysical Research…
2011
Corpus ID: 23677083
2010
2010
Ectodermal dysplasia‐like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome
L. Rifai
,
M. Port-Lis
,
+7 authors
A. Aboura
American Journal of Medical Genetics. Part A
2010
Corpus ID: 40523810
We report on a patient with an interstitial deletion of the long arm of chromosome 2 at 2q31.2q33.2. She had prenatal and…
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