[1]
P. Vishwakarma, A. Dubey, D. Kalo, and V. Mishra, “Identification of a novel mutation (c.1172_1181 del TGGTGCAAGC (p.Leu391fs) in the CUL7 gene in a patient of 3M Syndrome”, Polymorphism, vol. 9, pp. 17-22, Jun. 2022.