Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference98 articles.
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4. 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia;Karayiorgou;Nat. Rev. Neurosci,2010
5. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes;Meechan;Int. J. Dev. Neurosci,2011
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