Whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy: A case report of an Indian family

Por Gupta, Shashank, Chaurasia, Amit, Pathak, Ekta, Mishra, Rajeev, Chaudhry, Vidya Nair, Chaudhry, Prashaant, Mukherjee, Ashim, Mutsuddi, Mousumi
Publicado no Medicine (Baltimore) (2017)

MTHFR C677T Predisposes to POAG but Not to PACG in a North Indian Population: A Case Control Study

Por Gupta, Shashank, Bhaskar, Pradeep Kumar, Bhardwaj, Ritu, Chandra, Abhishek, Chaudhry, Vidya Nair, Chaudhry, Prashaant, Ali, Akhtar, Mukherjee, Ashim, Mutsuddi, Mousumi
Publicado em 2014