Association between aplastic anaemia and mutations in telomerase RNA

Lancet

Volumn 359, Issue 9324, 2002, Pages 2168-2170

  Vulliamy, Tom ^a   Marrone, Anna ^a   Dokal, Inderjeet ^a   Mason, Philip J ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOSTEROID; CYCLOSPORIN; OXYMETHOLONE; RNA; TELOMERASE;

ADOLESCENT; ADULT; APLASTIC ANEMIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DYSKERATOSIS CONGENITA; FAMILY HISTORY; FEMALE; GENE MUTATION; GERM LINE; HUMAN; INFANT; MALE; PRIORITY JOURNAL; STEM CELL TRANSPLANTATION; TELOMERE;

EID: 0037157582     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(02)09087-6     Document Type: Article

References (5)

1. The etiology of acquired aplastic anemia
2. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
3. Progressive telomere shortening in aplastic anemia
4. Secondary structure of vertebrate telomerase RNA
5. Mammalian telomeres and telomerase