MRX87 family with <it>Aristaless X </it>dup24bp mutation and implication for polyAlanine expansions

• Main Authors: D'Urso Michele (Author), Neri Giovanni (Author), Ventruto Valerio (Author), D'Eustacchio Angela (Author), Maiorino Antonio (Author), Monfregola Jlenia (Author), D'Adamo Pio (Author), Spizzichino Letizia (Author), Laperuta Carmela (Author), Chiurazzi Pietro (Author), Ursini Matilde (Author), Miano Maria (Author)
• Format: Book
• Published: BMC, 2007-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>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 <it>Aristaless related homeobox </it>(<it&g...