Novel compound heterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma

By Ohtake Yuichiro   Kubota Ryo   Tanino Tomihiko   Miyata Hiroshi   Mashima Yukihiko  

Ophthalmic Genetics, Vol. 21, Iss. 3, 2000-09 ,pp. : 191-193

Informa Healthcare

Access to resources Recommend Favorite

LTBP2 gene analysis in the GLC3C -linked family and 94 CYP1B1 -negative cases with primary congenital glaucoma

By Sharafieh Roshanak   Child Anne H.  

Ophthalmic Genetics, Vol. 34, Iss. 1-2, 2013-06 ,pp. : 14-20

Informa Healthcare

Access to resources Recommend Favorite

Novel Homozygous CYP1B1 Deletion in Siblings with Primary Congenital Glaucoma

By Damjanovich Kristy   Baldwin Erin E.   Lewis Tracey   Bayrak-Toydemir Pinar  

Ophthalmic Genetics, Vol. 34, Iss. 3, 2013-09 ,pp. : 180-181

Informa Healthcare

Access to resources Recommend Favorite

Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador

By Curry Stacey M.   Daou Aline G.   Hermanns Pia   Molinari Andrea   Lewis Richard Alan   Bejjani Bassem A.  

Ophthalmic Genetics, Vol. 25, Iss. 1, 2004-03 ,pp. : 3-9

Informa Healthcare

Access to resources Recommend Favorite

Identification of Novel Mutations in the XLRS1 Gene in Chinese Patients with X-linked Juvenile Retinoschisis

By Zeng Meizhen   Yi Changxian   Guo Xiangming   Jia Xiaoyun   Deng Yan   Wang Juan   Shen Huangxuan  

Current Eye Research, Vol. 32, Iss. 7-8, 2007-02 ,pp. : 685-691

Informa Healthcare

Access to resources Recommend Favorite