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    Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A

    Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A by Juan Antonio García-Carmona, Matthew J. Yousefzadeh, Fernando Alarcón-Soldevilla, Eva Fages-Caravaca, Eva Fages-Caravaca, Tra L. Kieu, Mariah A. Witt, Ángel López-Ávila, Laura J. Niedernhofer, José Antonio Pérez-Vicente

    Published 2021-08-01
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