108
Views
4
CrossRef citations to date
0
Altmetric
Letters to the Journal

A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing

, , , , , , , , , & show all

References

  • Reddy MA, Francis PJ, Berry V, et al. Molecular genetic basis of inherited cataract and associated phenotypes. Surv Ophthal 2004;49(3):300–315.
  • Alcalá J, Lieska N, Maisel H. Protein composition of bovine lens cortical fiber cell membranes. Exp Eye Res 1975;21(6):581–595.
  • Berry V, Francis P, Kaushal S, et al. Missense mutations in MIP underlie autosomal dominant ‘polymorphic’ and lamellar cataracts linked to 12q. Nature Genet 2000;25(1):15–17.
  • Geyer DD, Spence MA, Johannes M, et al. Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract. Am J Ophthalmol 2006;141(4):761–761.
  • Kumar GS, Kyle JW, Minogue PJ, et al. An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract. Exp Eye Res 2012;110(5):136–141.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.