Telomere shortening by mutations in theRTEL1helicase cause severe form of dyskeratosis congenita, Hoyerall-Hreidarsson syndrome

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Abstract

Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenital

Ballew et al. (2013)

Journal of Human Genetics 132: 473–480.

Constitutional mutations in RTEL1 cause severe dyskeratosis congenita

Walne et al. (2013)

American Journal of Human Genetics 92 (3): 448–453.

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