Cockayne syndrome: A pediatric neurodegenerative disorder linking mitochondria to aging.

Hatch, Mary Kate; Donnelly, Colleen; Prasun, Pankaj

Hatch, Mary Kate; Donnelly, Colleen; Prasun, Pankaj.

Hatch MK; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA.
Donnelly C; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA.
Prasun P; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA. Electronic address: Pankaj.prasun@mssm.edu.

J Neurol Sci ; 457: 122863, 2024 Feb 15.

Article en En | MEDLINE | ID: mdl-38190785

Asunto(s)

Síndrome de Cockayne; Humanos; Niño; Síndrome de Cockayne/complicaciones; Síndrome de Cockayne/genética; Envejecimiento; Daño del ADN; Mitocondrias; Enzimas Reparadoras del ADN/genética

Palabras clave

Aging; Cockayne syndrome; DNA repair; Mitochondria; Neurodegeneration

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Cockayne Límite: Child / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo

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PubMed Links

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Cockayne Límite: Child / Humans Idioma: En Año: 2024 Tipo del documento: Article