Related references
Note: Only part of the references are listed.Effectiveness of a Short Message Reminder in Increasing Compliance with Pediatric Cataract Treatment A Randomized Trial
Haotian Lin et al.
OPHTHALMOLOGY (2012)
Novel β-Crystallin Gene Mutations in Chinese Families With Nuclear Cataracts
Kai Jie Wang et al.
ARCHIVES OF OPHTHALMOLOGY (2011)
Molecular characteristics of inherited congenital cataracts
Bingyu Huang et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2010)
A novel mutation in CRYBB2 responsible for inherited coronary cataract
D. Lou et al.
EYE (2009)
Autosomal-Dominant Cerulean Cataract in a Chinese Family Associated with Gene Conversion Mutation in Beta-B2-Crystallin
Li Wang et al.
OPHTHALMIC RESEARCH (2009)
Congenital cataracts and their molecular genetics
J. Fielding Hejtmancik
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2008)
Crystallins in the eye: Function and pathology
Usha P. Andley
PROGRESS IN RETINAL AND EYE RESEARCH (2007)
Deamidation in human lens βB2-crystallin destabilizes the dimer
KJ Lampi et al.
BIOCHEMISTRY (2006)
Mutation analysis of congenital cataracts in Indian families:: Identification of SNPs and a new causative allele in CRYBB2 gene
ST Santhiya et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2004)
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract
MA Reddy et al.
HUMAN MOLECULAR GENETICS (2004)
Molecular genetic basis of inherited cataract and associated phenotypes
MA Reddy et al.
SURVEY OF OPHTHALMOLOGY (2004)
A unique form of autosomal dominant cataract explained by gene conversion between β-crystallin B2 and its pseudogene
Vanita et al.
JOURNAL OF MEDICAL GENETICS (2001)
Two interactive genes responsible for a new inherited cataract (RCT) in the mouse
YY Maeda et al.
MAMMALIAN GENOME (2001)
Human lens β-crystallin solubility
JH Feng et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
