Related content

Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human β-Crystallin Gene CRYBB2

By Litt Michael  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 665-668

Oxford University Press

Access to resources Recommend Favorite

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

By Litt M.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 471-474

Oxford University Press

Access to resources Recommend Favorite

A 1-bp deletion in the C-crystallin leads to dominant cataracts in mice

By Zhao Liya  

Mammalian Genome, Vol. 21, Iss. 7-8, 2010-08 ,pp. : 361-369

Springer Publishing Company

Access to resources Recommend Favorite

A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family

By Qi Yanhua   Jia Hongyan   Huang Shangzhi   Lin Hui   Gu Jingzhi   Su Hong   Zhang Tieying   Gao Ya   Qu Lijun   Li Dandan   Li Ying  

Human Genetics, Vol. 114, Iss. 2, 2004-01 ,pp. : 192-197

Springer Publishing Company

Access to resources Recommend Favorite

Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract

By  

Molecular Syndromology, Vol. 7, Iss. 2, 2016-04 ,pp. : 87-92

Karger

Access to resources Recommend Favorite