Pages that link to "Q34597155"

The following pages link to Progressive sutural cataract associated with a BFSP2 mutation in a Chinese family. (Q34597155):

Displaying 15 items.

• GFAP and its role in Alexander disease (Q24657223) (← links)
• Tmod1 and CP49 synergize to control the fiber cell geometry, transparency, and mechanical stiffness of the mouse lens (Q28863029) (← links)
• A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family (Q34217327) (← links)
• A G→T splice site mutation of CRYBA1/A3 associated with autosomal dominant suture cataracts in a Chinese family (Q35166634) (← links)
• Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA (Q35531741) (← links)
• Lens ion homeostasis relies on the assembly and/or stability of large connexin 46 gap junction plaques on the broad sides of differentiating fiber cells (Q35622426) (← links)
• Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis) (Q36251461) (← links)
• A novel mutation in CRYAA is associated with autosomal dominant suture cataracts in a Chinese family (Q36499609) (← links)
• Insights into the beaded filament of the eye lens (Q36816245) (← links)
• A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts. (Q36950476) (← links)
• Congenital cataracts and their molecular genetics (Q37012783) (← links)
• A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea (Q37083758) (← links)
• Lens intermediate filaments (Q37227723) (← links)
• Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis (Q39370800) (← links)
• Identification of long non-coding RNA and mRNA expression in βΒ2-crystallin knockout mice. (Q55237423) (← links)