Citations for
1CRYABB, CPP2
A novel alphaB-crystallin mutation associated with autosomal dominant congenital lamellar cataract.
Liu Y, Zhang X, Luo L, Wu M, Zeng R, Cheng G, Hu B, Liu B, Liang JJ, Shang F.
Invest Ophthalmol Vis Sci 47(3):1069-75. 2006
2CPP2, CRYAB
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.
Berry V, Francis P, Reddy MA, Collyer D, Vithana E, MacKay I, Dawson G, Carey AH, Moore A, Bhattacharya SS, Quinlan RA.
Am J Hum Genet 69(5):1141-5. 2001