Karuthedath Vellarikkal, S., Jayarajan, R., Verma, A., Nair, S., Ravi, R., Senthivel, V., . . . Scaria, V. (2016). Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa. F1000Res.

Karuthedath Vellarikkal, Shamsudheen, Rijith Jayarajan, Ankit Verma, Sreelata Nair, Rowmika Ravi, Vigneshwar Senthivel, Sridhar Sivasubbu, and Vinod Scaria. "Case Report: Whole Exome Sequencing Reveals a Novel Frameshift Deletion Mutation P.G2254fs in COL7A1 Associated With Autosomal Recessive Dystrophic Epidermolysis Bullosa." F1000Res 2016.

Karuthedath Vellarikkal, Shamsudheen, et al. "Case Report: Whole Exome Sequencing Reveals a Novel Frameshift Deletion Mutation P.G2254fs in COL7A1 Associated With Autosomal Recessive Dystrophic Epidermolysis Bullosa." F1000Res 2016.