A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice

Author:

Sidjanin D.J.,Parker-Wilson Devonne M.,Neuhäuser-Klaus Angelika,Pretsch Walter,Favor Jack,Deen Peter M.T.,Ohtaka-Maruyama Chiaki,Lu Yun,Bragin Alvina,Skach William R.,Chepelinsky Ana B.,Grimes Patricia A.,Stambolian Dwight E.

Publisher

Elsevier BV

Subject

Genetics

Reference36 articles.

1. Al-Ghoul, K, Kuszak, J, Friedrich, G, and, Shiels, A. 1999, The Structure of Mip26 Knockout Mouse Lenses, US–Japan Cooperative Cataract Research Group Meeting, S-4.1.

2. Short Protocols in Molecular Biology;Ausubel,1992

3. Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q;Berry;Nat. Genet.,2000

4. Activation of the γE-crystallin pseudogene in the human hereditary Coppock-like cataract;Brakenhoff;Hum. Mol. Genet.,1994

5. Lens membranes II. Isolation and characterization of the main intrinsic polypeptide (MIP) of bovine lens fiber membranes;Broekhuyse;Exp. Eye Res.,1976

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