S-EPMC10389160 - 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. - OmicsDI

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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.

ABSTRACT:

SUBMITTER: Srikumar A

PROVIDER: S-EPMC10389160 | biostudies-literature | 2023 May-Jun

REPOSITORIES: biostudies-literature