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Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene

Heterozygous mutations in the telomerase components TERT, the reverse transcriptase, and TERC, the RNA template, cause autosomal dominant dyskeratosis congenita due to telomere shortening. Anticipation, whereby the disease severity increases in succeeding generations due to inheritance of shorter te...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Du, Hong-Yan, Pumbo, Elena, Manley, Peter, Field, Joshua J., Bayliss, Susan J., Wilson, David B., Mason, Philip J., Bessler, Monica
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society of Hematology 2008
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2214749/
https://ncbi.nlm.nih.gov/pubmed/18042801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2007-10-120907
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