Author:
Currò Aurora,Doddato Gabriella,Bruttini Mirella,Zollino Marcella,Marangi Giuseppe,Zappella Michele,Renieri Alessandra,Pinto Anna Maria
Subject
Genetics(clinical),Genetics,General Medicine
Reference21 articles.
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3. Transcription factor 4 and myocyte enhancer factor 2C mutations are not common causes of Rett syndrome;Armani;Christodoulou J. Am J Med Genet A,2012
4. Severe mental retardation with breathing abnormalities (Pitt–Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4;Brockschmidt;Hum. Mol. Genet.,2007
5. A novel CDKL5 mutation in a Japanese patient with atypical Rett syndrome;Christianto;Clin. Chim. Acta,2016
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