Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma-Reference-Cited by-同舟云学术

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

Published:2009-08-04 Issue:20 Volume:18 Page:3969-3977
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Narooie-Nejad Mehrnaz,Paylakhi Seyed Hassan,Shojaee Seyedmehdi,Fazlali Zeinab,Rezaei Kanavi Mozhgan,Nilforushan Naveed,Yazdani Shahin,Babrzadeh Farbod,Suri Fatemeh,Ronaghi Mostafa,Elahi Elahe,Paisán-Ruiz Coro

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/20/3969/17248031/ddp338.pdf

Reference49 articles.

1. Gene mapping for primary open angle glaucoma;Fan;Clin. Biochem.,2006

2. Recent advances in molecular genetics of glaucoma;Ray;Mol. Cell. Biochem.,2003

3. Recent advances in molecular genetics of glaucomas;Sarfarazi;Hum.Mol. Genet.,1997

4. Number of people with glaucoma worldwide;Quigley;Br. J. Ophthalmol.,1996

5. Genetics and biochemistry of primary congenital glaucoma;Sarfarazi;Ophthalmol. Clin. North Am.,2003

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