Impact of germline CTC1 alterations on telomere length in acquired bone marrow failure

Compound heterozygous germline mutations in CTC1 gene have been found in patients with atypical dyskeratosis congenita (DC), whereas heterozygous carriers are unaffected. Through screening of a large cohort of adult patients with acquired bone marrow failure syndromes, in addition to a DC case, we h...

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Detalhes bibliográficos
Publicado no:Br J Haematol
Main Authors: Shen, Wenyi, Kerr, Cassandra M., Przychozen, Bartlomiej, Mahfouz, Reda Z., LaFramboise, Thomas, Nagata, Yasunobu, Hanna, Rabi, Radivoyevitch, Tomas, Nazha, Aziz, Sekeres, Mikkael A., Maciejewski, Jaroslaw P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6536344/
https://ncbi.nlm.nih.gov/pubmed/30891747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjh.15862
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