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

印度人群中新生儿罕见遗传性皮肤病Kindler综合征的基因诊断：发现FERMT1基因中存在无义突变c.328C>T