Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Srikrupa N Natarajan"'
Autor:
Dhandayuthapani Sudha, Srividya Neriyanuri, Ramya Sachidanandam, Srikrupa N Natarajan, Mamatha Gandra, Arokiasamy Tharigopala, Muthukumaran Sivashanmugam, Mohammed Alameen, Umashankar Vetrivel, Lingam Gopal, Vikas Khetan, Rajiv Raman, Parveen Sen, Subbulakshmi Chidambaram, Jayamuruga Pandian Arunachalam
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0198086 (2018)
X-linked retinoschisis (XLRS) is a retinal degenerative disorder caused by mutations in RS1 gene leading to splitting of retinal layers (schisis) which impairs visual signal processing. Retinoschisin (RS1) is an adhesive protein which is secreted pre
Externí odkaz:
https://doaj.org/article/8d9a99cf407c4c54b57681d629ae9366
Autor:
Pradeep T Manchegowda, Srikrupa N. Natarajan, Puja Maitra, Parveen Sen, Srivatsan Sripriya, Sinnakaruppan Mathavan, Muna Bhende
Publikováno v:
Ophthalmic Genetics. 41:570-578
Mutations inA retrospective analysis was performed in 28 eyes of the 14 unrelated patients to establish genotype phenotype correlation. Targeted next generation sequencing was performed using the STRAND® NGS v2.5 software. Validation was done using
Autor:
Srividya Neriyanuri, Mamatha Gandra, Arokiasamy Tharigopala, Lingam Gopal, Jayamuruga Pandian Arunachalam, Vikas Khetan, Srikrupa N. Natarajan, Mohammed Alameen, Muthukumaran Sivashanmugam, Parveen Sen, Ramya Sachidanandam, Rajiv Raman, Dhandayuthapani Sudha, Umashankar Vetrivel, Subbulakshmi Chidambaram
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0198086 (2018)
PLoS ONE
PLoS ONE
X-linked retinoschisis (XLRS) is a retinal degenerative disorder caused by mutations in RS1 gene leading to splitting of retinal layers (schisis) which impairs visual signal processing. Retinoschisin (RS1) is an adhesive protein which is secreted pre