Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
Le Guen T; Jullien L; Touzot F; Schertzer M; Gaillard L; Perderiset M; Carpentier W; Nitschke P; Picard C; Couillault G; Soulier J; Fischer A; Callebaut I; Jabado N; Londono-Vallejo A; de Villartay JP; Revy P; Human Molecular Genetics, 2013, vol. 22, issue 16, p 3239, ISSN 14602083. ISBN 14602083.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef