Telomere dysfunction in human bone marrow failure syndromes.
about
ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function.The diagnosis and treatment of dyskeratosis congenita: a review.Telomere length assessment in leukocytes presents potential diagnostic value in patients with breast cancerFunctional characterization of human CTC1 mutations reveals novel mechanisms responsible for the pathogenesis of the telomere disease Coats plus.
P2860
Telomere dysfunction in human bone marrow failure syndromes.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Telomere dysfunction in human bone marrow failure syndromes.
@en
Telomere dysfunction in human bone marrow failure syndromes.
@nl
type
label
Telomere dysfunction in human bone marrow failure syndromes.
@en
Telomere dysfunction in human bone marrow failure syndromes.
@nl
prefLabel
Telomere dysfunction in human bone marrow failure syndromes.
@en
Telomere dysfunction in human bone marrow failure syndromes.
@nl
P2860
P356
P1433
P1476
Telomere dysfunction in human bone marrow failure syndromes.
@en
P2093
Ludmila Shtessel
Shawn Ahmed
P2860
P356
10.4161/NUCL.13993
P577
2011-01-01T00:00:00Z