MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions

BACKGROUND: Cognitive impairments are heterogeneous conditions, and it is estimated that 10% may be caused by a defect of mental function genes on the X chromosome. One of those genes is Aristaless related homeobox (ARX) encoding a polyA-rich homeobox transcription factor essential for cerebral patt...

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Bibliographic Details
Main Authors: Laperuta, Carmela, Spizzichino, Letizia, D'Adamo, Pio, Monfregola, Jlenia, Maiorino, Antonio, D'Eustacchio, Angela, Ventruto, Valerio, Neri, Giovanni, D'Urso, Michele, Chiurazzi, Pietro, Ursini, Matilde Valeria, Miano, Maria Giuseppina
Format: Artigo
Language:Inglês
Published: BioMed Central 2007
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1868705/
https://ncbi.nlm.nih.gov/pubmed/17480217
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-25
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