Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita.
Leukemia
; 32(8): 1762-1767, 2018 08.
Article
in En
| MEDLINE
| ID: mdl-29749397
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myelodysplastic Syndromes
/
Leukemia, Myeloid, Acute
/
Biomarkers, Tumor
/
Dyskeratosis Congenita
/
Telomere Shortening
/
Mutation
Type of study:
Incidence_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Europa
Language:
En
Journal:
Leukemia
Journal subject:
HEMATOLOGIA
/
NEOPLASIAS
Year:
2018
Document type:
Article
Affiliation country:
Germany
Country of publication:
United kingdom