PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population

Παρόμοια τεκμήρια

• Novel mutations associated with autosomal-dominant congenital cataract identified in Chinese families
  ανά: Wang, Zhenyu, κ.ά.
  Έκδοση: (2019)
• Novel mutations in CRYGC are associated with congenital cataracts in Chinese families
  ανά: Zhong, Zilin, κ.ά.
  Έκδοση: (2017)
• Connexin46 mutations in autosomal dominant congenital cataract.
  ανά: Mackay, D, κ.ά.
  Έκδοση: (1999)
• Novel mutation of GJA8 in autosomal dominant congenital cataracts
  ανά: Ding, Ning, κ.ά.
  Έκδοση: (2020)
• Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract
  ανά: Ma, Z, κ.ά.
  Έκδοση: (2005)