Dyskeratosis congenita and the DNA damage response

Παρόμοια τεκμήρια

• Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita
  ανά: Vulliamy, Tom, κ.ά.
  Έκδοση: (2008)
• TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes
  ανά: Walne, Amanda J., κ.ά.
  Έκδοση: (2008)
• Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome
  ανά: Walne, Amanda J., κ.ά.
  Έκδοση: (2010)
• Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
  ανά: Walne, Amanda J., κ.ά.
  Έκδοση: (2013)
• Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome
  ανά: Marrone, Anna, κ.ά.
  Έκδοση: (2007)