In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma-Reference-Cited by-同舟云学术

In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma

Published:2017-04-06 Issue:2 Volume:38 Page:807-814
ISSN:0165-5701
Container-title:International Ophthalmology
language:en
Short-container-title:Int Ophthalmol

Author:

Firasat Sabika,Kaul Haiba,Ashfaq Usman Ali,Idrees Sobia

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Link

http://link.springer.com/article/10.1007/s10792-017-0508-4/fulltext.html

Reference38 articles.

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2. Cascella R, Strafella C, Germani C, Novelli G, Ricci F, Zampatti S, Giardina E (2015) The genetics and the genomics of primary congenital glaucoma. Biomed Res Int 2015:321291

3. Sarfarazi M, Akarsu AN, Hossain A, Turacli ME, Aktan SG, Barsoum-Homsy M, Chevrette L, Sayli BS (1995) Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 30:171–177

4. Ho CL, Walton DS (2004) Primary congenital glaucoma: 2004 update. J Pediatr Ophthalmol Strabismus 41:271–288

5. Wiggs JL (2007) Genetic etiologies of glaucoma. Arch Ophthalmol 125:30–37

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