Mutations in the chromatin-associated protein ATRX.

Ítems similars

• Partial rescue of truncating mutations in the ATRX gene through unusual intra-exonic splicing
  per: Malik, N, et al.
  Publicat: (2006)
• A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
  per: Steensma, D, et al.
  Publicat: (2004)
• Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
  per: Steensma, D, et al.
  Publicat: (2004)
• Functional significance of mutations in the Snf2 domain of ATRX.
  per: Mitson, M, et al.
  Publicat: (2011)
• Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
  per: Argentaro, A, et al.
  Publicat: (2007)