Towards a unified cellular role for the Axenfeld-Rieger malformation genes PITX2 and FOXC1

• Author / Creator

  Lines, Matthew Alexander

• Subjects / Keywords

  • Axenfeld-Rieger syndrome. Genetic aspects.
  • Eye. Abnormalities. Etiology.
  • Transcription factors.
  • Recombinant proteins.

• Graduation date

  2004

• Type of Item

  Thesis

• Degree

  Master of Science

• DOI

  https://doi.org/10.7939/r3-904x-dt67

• License

  This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for the purpose of private, scholarly or scientific research. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.