Intracellular distribution of a speech/language disorder associated FOXP2 mutant

This publication has 27 references indexed in Scilit:

• FOXP2 and the neuroanatomy of speech and language
  Nature Reviews Neuroscience, 2005
• Fox's in development and disease
  Trends in Genetics, 2003
• A forkhead-domain gene is mutated in a severe speech and language disorder
  Nature, 2001
• Characterization of a New Subfamily of Winged-helix/Forkhead (Fox) Genes That Are Expressed in the Lung and Act as Transcriptional Repressors
  Journal of Biological Chemistry, 2001
• Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
  Human Molecular Genetics, 2001
• The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
  Nature Genetics, 2001
• X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
  Nature Genetics, 2001
• Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome
  American Journal of Human Genetics, 2000
• Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
  Nature Genetics, 1998
• The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
  Nature Genetics, 1998