Molecular insight of dyskeratosis congenita: Defects in telomere length homeostasis

BACKGROUND: Dyskeratosis congenita (DC) is a rare disease and is a heterogenous disorder, with its inheritance patterns as autosomal dominant, autosomal recessive, and X-linked recessive. This disorder occurs due to faulty maintenance of telomeres in stem cells. This congenital condition is diagnose...

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Detalles Bibliográficos
Autores principales: Dorgaleleh, Saeed, Naghipoor, Karim, Hajimohammadi, Zahra, Dastaviz, Farzad, Oladnabi, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Whioce Publishing Pte. Ltd. 2022
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791241/
https://www.ncbi.nlm.nih.gov/pubmed/35097237

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791241/
https://www.ncbi.nlm.nih.gov/pubmed/35097237

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