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CATARACT, MARNER TYPE

Known as: Zonular cataract, Cataract, zonular, Cataract, lamellar 
Zonular cataracts are defined to be cataracts that affect specific regions of the lens. [HPO:probinson, HPO:vkumar, pmid:18035564]
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Cataract

Narrower (1)

Congenital lamellar cataract

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Mutation causing self-aggregation in human gammaC-crystallin leading to congenital cataract.
PURPOSE Many forms of congenital hereditary cataract are associated with mutations in the crystallin genes. The authors focus… 
2006
2006
Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.
PURPOSE The molecular characterization of 27 members of an Indian family, with 13 members in four generations, affected with Y… 
2005
2005
Major histocompatibility complex-linked diabetes susceptibility in NOD/Lt mice: subcongenic analysis localizes a component of Idd16 at the H2-D end of the diabetogenic H2(g7) complex.
The diabetogenic major histocompatibility complex (MHC) (H2(g7)) of NOD mice comprises contributions from several class II loci… 
2005
2005
Crystallin {gamma}B-I4F mutant protein binds to {alpha}-crystallin and affects lens transparency.
A new mouse mutant line, Clapper, identified from N-ethyl-N-nitrosurea (ENU)-mutagenized mice, develops a dominant lamellar… 
2004
2004
Autosomal dominant coralliform cataract related to a missense mutation of the gammaD-crystallin gene.
BACKGROUND Congenital cataract is a sight-threatening disease that affects about 1 - 6 cases per 10000 live births and causes 10… 
Highly Cited
1999
Highly Cited
1999
Molecular mechanism underlying a Cx50-linked congenital cataract.
Mutations in gap junctional channels have been linked to certain forms of inherited congenital cataract (D. Mackay, A. Ionides, V… 
1998
1998
Nucleus fragmentation in a scleral pocket for small incision extracapsular cataract extraction
Highly Cited
1995
Highly Cited
1995
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.
Congenital cataracts constitute a morphologically and genetically heterogeneous group of diseases that are a major cause of… 
Highly Cited
1995
Highly Cited
1995
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36
Congenital cataract, type Volkmann (McKusick no 115665, gene symbol CCV) is an autosomal dominant eye disease. The disease is… 
Highly Cited
1994
Highly Cited
1994
The catechol 2,3-dioxygenase gene of Rhodococcus rhodochrous CTM: nucleotide sequence, comparison with isofunctional dioxygenases and evidence for an active-site histidine.
In cell-free extracts of Escherichia coli clones harbouring the 3.5 kb Bg/II fragment of plasmid pTC1 from Rhodococcus… 
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