De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability.

[1]  P. Gasparini,et al.  De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature. , 2012, European journal of medical genetics.

[2]  Hans van Bokhoven,et al.  Genetic and epigenetic networks in intellectual disabilities. , 2011, Annual review of genetics.

[3]  Christina L. Vizcarra,et al.  Structure and function of the interacting domains of Spire and Fmn-family formins , 2011, Proceedings of the National Academy of Sciences.

[4]  R. Huganir,et al.  Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. , 2011, American journal of human genetics.

[5]  M. Katoh,et al.  Characterization of FMN2 gene at human chromosome 1q43. , 2004, International Journal of Molecular Medicine.

[6]  S. Zigmond.  Formin-induced nucleation of actin filaments. , 2004, Current opinion in cell biology.

[7]  P. Leder,et al.  Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouse oocytes , 2002, Nature Cell Biology.

[8]  Charles Boone,et al.  Role of Formins in Actin Assembly: Nucleation and Barbed-End Association , 2002, Science.

[9]  A. Yamanaka,et al.  Mice lacking the M3 muscarinic acetylcholine receptor are hypophagic and lean , 2001, Nature.

[10]  P. Leder,et al.  Formin-2, a novel formin homology protein of the cappuccino subfamily, is highly expressed in the developing and adult central nervous system , 2000, Mechanisms of Development.

[11]  Liqun Luo,et al.  Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity. , 2002, Annual review of cell and developmental biology.