Associated Papers
Two novel mutations in KIND1 in Indian patients with Kindler syndrome.
Kantheti P et al.
Clinical and Experimental Dermatology, 2017
Genetic Diagnosis of Kindler Syndrome, a Rare form of Genodermatosis in a Newborn with Identification of a Nonsense Mutation, c. 328C > T, in the FERMT1 Gene in the Indian Population.
Srikumar A et al.
Indian Journal of Dermatology, 0
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