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, و 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.