Cargando…
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...
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: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791241/ https://www.ncbi.nlm.nih.gov/pubmed/35097237 |
Ejemplares similares
-
Are Dyskeratosis Congenita patients at higher risk of symptomatic COVID-19?
por: Dorgaleleh, Saeed, et al.
Publicado: (2022) -
Dyskeratosis congenita, stem cells and telomeres
por: Kirwan, Michael, et al.
Publicado: (2009) -
The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenita
por: Gadalla, Shahinaz M., et al.
Publicado: (2016) -
Long tails, short telomeres: Dyskeratosis congenita
por: Tummala, Hemanth, et al.
Publicado: (2015) -
Dyskeratosis congenita
por: Gitto, Lorenzo, et al.
Publicado: (2020)