APA استشهاد

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.

استشهاد بنمط شيكاغو

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.

MLA استشهاد

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.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.