Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations

BACKGROUND: Cockayne syndrome (CS) is a rare autosomal recessive disorder caused by mutations in ERCC6/CSB or ERCC8/CSA that participate in the transcription-coupled nucleotide excision repair (TC-NER) of UV-induced DNA damage. CS patients display a large heterogeneity of clinical symptoms and sever...

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Detalles Bibliográficos
Autores principales: Chikhaoui, Asma, Kraoua, Ichraf, Calmels, Nadège, Bouchoucha, Sami, Obringer, Cathy, Zayoud, Khouloud, Montagne, Benjamin, M’rad, Ridha, Abdelhak, Sonia, Laugel, Vincent, Ricchetti, Miria, Turki, Ilhem, Yacoub-Youssef, Houda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898519/
https://www.ncbi.nlm.nih.gov/pubmed/35248096
http://dx.doi.org/10.1186/s13023-022-02257-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898519/
https://www.ncbi.nlm.nih.gov/pubmed/35248096
http://dx.doi.org/10.1186/s13023-022-02257-1

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