A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes - Archive ouverte HAL Access content directly
Journal Articles American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Year : 2006

A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes

Faisal Idrees
  • Function : Author
Samantha Free
  • Function : Author
Daniela Vaideanu
  • Function : Author
Pamela Thompson
  • Function : Author
Paul Ashley
  • Function : Author
Glen Brice
  • Function : Author
Paul Rutland
  • Function : Author
Maria Bitner-Glindzicz
  • Function : Author
Peng Khaw
  • Function : Author
Scott Fraser
  • Function : Author
Sanjay Sisodiya
  • Function : Author
Jane Sowden
  • Function : Author

Domains

Genetics

Dates and versions

hal-04093299 , version 1 (10-05-2023)

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Faisal Idrees, Agnes Bloch-Zupan, Samantha Free, Daniela Vaideanu, Pamela Thompson, et al.. A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2006, 141B (2), pp.184-191. ⟨10.1002/ajmg.b.30237⟩. ⟨hal-04093299⟩
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