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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

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Bibliographic Details
Published in:	Frontiers in genetics 2021, Vol.12, p.717361-717361
Main Authors:	García-Carmona, Juan Antonio, Yousefzadeh, Matthew J, Alarcón-Soldevilla, Fernando, Fages-Caravaca, Eva, Kieu, Tra L, Witt, Mariah A, López-Ávila, Ángel, Niedernhofer, Laura J, Pérez-Vicente, José Antonio
Format:	Report
Language:	English
Online Access:	Get full text
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