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#PubSaludMurcia Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A. @Area2Cartagena https://t.co/vZ3BQylrpY
#PubSaludMurcia Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A. @Area2Cartagena https://t.co/vZ3BQylrpY
New Research: Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A: We aimed to determine if an adolescent patient presenting with… https://t.co/Lz