Hemizygous Deletion of the Syntaxin 1A Gene in Individuals with Williams Syndrome

This publication has 22 references indexed in Scilit:

• Neuropsychological, neurological, and neuroanatomical profile of Williams syndrome
  American Journal of Medical Genetics, 2005
• Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients
  Genomics, 1996
• LIM–kinase deleted in Williams syndrome
  Nature Genetics, 1996
• Calcium-dependent interaction of N-type calcium channels with the synaptic core complex
  Nature, 1996
• Cloning and sequence analysis of a cDNA encoding human syntaxin 1A, a polypeptide essential for exocytosis
  Gene, 1995
• Williams syndrome: Autosomal dominant inheritance
  American Journal of Medical Genetics, 1993
• The Williams syndrome: Evidence for possible autosomal dominant inheritance
  American Journal of Medical Genetics, 1993
• Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
  Nature Genetics, 1993
• Syntaxin: A Synaptic Protein Implicated in Docking of Synaptic Vesicles at Presynaptic Active Zones
  Science, 1992
• Williams syndrome professional symposium
  American Journal of Medical Genetics, 1990