Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype

Author： Zhang Qingjiong Li Shiqiang Guo Xiangming Guo Li Xiao Xueshan Jia Xiaoyun Kuang Zhihe

ISSN： 1381-6810

Source： Ophthalmic Genetics, Vol.22, Iss.2, 2001-06, pp. : 89-96

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Screening of the RPE65 Gene in the Asian Indian Patients with Leber Congenital Amaurosis

By Mamatha Gandra Srilekha Sundaramurthy Meenakshi Swaminathan Kumaramanickavel Govindasamy

Ophthalmic Genetics, Vol. 29, Iss. 2, 2008-06 ,pp. : 73-78

Informa Healthcare

Access to resources Recommend Favorite

Visual improvement in Leber congenital amaurosis and the CRX genotype

By Koenekoop Robert K. Loyer Magali Dembinska Olga Beneish Raquel

Ophthalmic Genetics, Vol. 23, Iss. 1, 2002-03 ,pp. : 49-59

Informa Healthcare

Access to resources Recommend Favorite

Mutational analysis and clinical correlation in Leber congenital amaurosis

By Dharmaraj Sharola Silva Eduardo Pina Ana Luisa Li Ying Ying Yang Jun-Ming Carter R. Colin Loyer Magali El-Hilali Hala Traboulsi Elias Sundin Olof Zhu Danping Koenekoop Robert K. Maumenee Irene H.

Ophthalmic Genetics, Vol. 21, Iss. 3, 2000-09 ,pp. : 135-150

Informa Healthcare

Access to resources Recommend Favorite

Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family

By Rezaie Tayebeh Karimi-Nejad Mohammad-Hassan Meshkat Mohammad-Reza Sohbati Saeed Karimi-Nejad Roxana Najmabadi Hossein Sarfarazi Mansoor

Ophthalmic Genetics, Vol. 28, Iss. 4, 2007-10 ,pp. : 224-228

Informa Healthcare

Access to resources Recommend Favorite

Analysis of three genes in Leber congenital amaurosis in Indonesian patients

By Sitorus R.S. Lorenz B. Preising M.N.

Vision Research, Vol. 43, Iss. 28, 2003-12 ,pp. : 3087-3093

Elsevier

Access to resources Recommend Favorite