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Nuclear pulverulent cataract

Known as: Central pulverulent cataract, Pulverulent nuclear cataract, cataracta pulverulenta centralis 
A type of nuclear cataract involving congenital pulverulent disc-like opacity of the embryonal and fetal nucleus. [HPO:probinson, pmid:10634616]
National Institutes of Health

Papers overview

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2016
2016
The cataract related mutation N188T in human connexin46 (hCx46) revealed a critical role for residue N188 in the docking process of gap junction channels.
Review
2015
Review
2015
Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis).
PURPOSE To assess for phenotype-genotype correlations in families with recessive pediatric cataract and identified gene mutations… 
2012
2012
Clinical and molecular analysis of children with central pulverulent cataract from the Arabian Peninsula
Aim To clinically and genetically characterise central pulverulent cataract in a consecutive cohort of children from the Arabian… 
2010
2010
First Report of Leaf Rust of Blueberry Caused by Thekopsora minima on Vaccinium corymbosum in the Western Cape, South Africa.
Southern highbush blueberry plants (Vaccinium corymbosum interspecific hybrids) showing rust-like symptoms were observed in July… 
2009
2009
Initiation codon mutation in βB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract
Purpose To identify the molecular basis for autosomal recessively inherited congenital non-syndromic pulverulent cataracts in a… 
2008
2008
A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract
Purpose To identify the genetic cause responsible for the autosomal dominant hereditary cataract in a Chinese family. Methods A… 
Highly Cited
2004
Highly Cited
2004
A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
PURPOSE To report the identification of a novel mutation of connexin46 in a large Chinese family with autosomal dominant… 
Highly Cited
2003
Highly Cited
2003
A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.
PURPOSE Autosomal dominant congenital cataract (ADCC) is a clinically and genetically heterogeneous lens disorder that usually… 
1984
1984
Syndrome d'Urrets-Zavalia et cataracta glaucomatosa
After penetrating keratoplasties for different congenital or acquired corneal diseases, the presence of characteristic cataracta… 
1975
1975
The glochidia of certain Unionidae (Mollusca) in Nova Scotia and their fish hosts.
  • M. Wiles
  • Canadian journal of zoology
  • 1975
  • Corpus ID: 46471321
Morphological and morphometric comparisons among adult and glochidial unionids from two Nova Scotian locations showed that… 
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