M. Mondal

Functional assessment of tyrosinase variants identified in individuals with albinism is essential for unequivocal determination of genotype‐to‐phenotype correlation

K. Ray, M. Sengupta, M. Mondal, 2016, The British journal of dermatology.

Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings.

K. Ray, M. Sengupta, S. Samanta, 2012, Gene.

Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patients.

K. Ray, M. Sengupta, Abhisek Bhattacharya, 2011, The Journal of investigative dermatology.

Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos

K. Ray, D. Sarkar, M. Sengupta, 2013, Journal of Genetics.

Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene

K. Ray, M. Sengupta, S. Samanta, 2010, The British journal of dermatology.