Ramachandran Ramya Devi

Summary

Affiliation: Aravind Eye Hospital

Country: India

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea
Ramachandran Ramya Devi
Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
Mol Vis 12:190-5. 2006
Crystallin gene mutations in Indian families with inherited pediatric cataract
Ramachandran Ramya Devi
Department of Genetics, Dr G Venketaswamy Eye Research Institute, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, India
Mol Vis 14:1157-70. 2008
Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population
Ramachandran Ramya Devi
Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
Mol Vis 11:846-52. 2005

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea
Ramachandran Ramya Devi
Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
Mol Vis 12:190-5. 2006
....
Crystallin gene mutations in Indian families with inherited pediatric cataract
Ramachandran Ramya Devi
Department of Genetics, Dr G Venketaswamy Eye Research Institute, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, India
Mol Vis 14:1157-70. 2008
..This study is aimed at identification of the spectrum and frequency of crystallin gene mutations in cataractous patients in an Indian population...
Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population
Ramachandran Ramya Devi
Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
Mol Vis 11:846-52. 2005
..The present study aimed to identify the spectrum of mutations in Connexin 46 in the Indian population...