Berry, V <br/><br/>
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family.  [electronic resource] 

 -  Eye (London, England)  04 2018 
 - 806-812 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1476-5454 
<br/><br/><label>Standard No.: </label>10.1038/eye.2017.268  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cataract--genetics<br/>Child<br/>Female<br/>Heat Shock Transcription Factors--genetics<br/>Humans<br/>Male<br/>Mutation, Missense<br/>Pedigree<br/>Exome Sequencing