Associated Papers
Novel MIP gene mutation causes autosomal-dominant congenital cataract.
Ni JL et al.
International Journal of Ophthalmology, 2024
A novel missense mutation in the gene encoding major intrinsic protein (MIP) in a Giant panda with unilateral cataract formation.
Bai C et al.
Bmc Genomics, 2021
The relationship between major intrinsic protein genes and cataract.
Sun W et al.
International Ophthalmology, 2021
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies.
Pippucci T et al.
Annals of Clinical and Translational Neurology, 2019
A novel MIP mutation in familial congenital nuclear cataracts.
Qin L et al.
European Journal of Medical Genetics, 2016
A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.
Yu Y et al.
Bmc Medical Genetics, 2014
A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract.
Ding X et al.
Plos One, 2014
A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family.
Zeng L et al.
Molecular Vision, 2013
A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.
Wang KJ et al.
Molecular Vision, 2011
A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.
Yang G et al.
Molecular Vision, 2011
Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP.
Xiao X et al.
Molecular Vision, 2011
A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family.
Wang W et al.
Molecular Vision, 2010
Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family.
Jiang J et al.
Molecular Vision, 2009
Molecular genetic basis of inherited cataract and associated phenotypes.
Reddy MA et al.
Survey of Ophthalmology, 0
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