Genomic Organization of the Human Gα14 and Gαq Genes and Mutation Analysis in Chorea–Acanthocytosis (CHAC)

This publication has 43 references indexed in Scilit:

• A Physical Map of 30,000 Human Genes
  Science, 1998
• Platelet signal transduction defect with Gα subunit dysfunction and diminished Gα _q in a patient with abnormal platelet responses
  Proceedings of the National Academy of Sciences, 1997
• Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion
  Science, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• Gene Structure of MurineGna11andGna15:Tandemly Duplicated Gq Class G Protein α Subunit Genes
  Genomics, 1996
• Molecular Cloning of Human Gαq cDNA and Chromosomal Localization of the Gαq Gene (GNAQ) and a Processed Pseudogene
  Genomics, 1995
• Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.
  Proceedings of the National Academy of Sciences, 1990
• Chorea-Acanthocytosis: Report of a Family and Neuropathological Study of Two Cases
  Canadian Journal of Neurological Sciences, 1989
• Ovalbumin gene: evidence for a leader sequence in mRNA and DNA sequences at the exon-intron boundaries.
  Proceedings of the National Academy of Sciences, 1978
• Familial degeneration of the basal ganglia with acanthocytosis: A clinical, neuropathological, and neurochemical study
  Annals of Neurology, 1978