A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing

Παρόμοια τεκμήρια

• A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein
  ανά: Zhang, Feng, κ.ά.
  Έκδοση: (2021)
• Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome
  ανά: Yin, Hou-fa, κ.ά.
  Έκδοση: (2014)
• Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome
  ανά: Valeria Lo Faro, κ.ά.
  Έκδοση: (2020-07-01)
• A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome
  ανά: Li, Dandan, κ.ά.
  Έκδοση: (2008)
• Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome
  ανά: Lo Faro, Valeria, κ.ά.
  Έκδοση: (2020)