A telomerase component is defective in the human disease dyskeratosis congenita

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Nature

• Publication date

  1999-12-02

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/990141PMID 10591218
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Telomere maintenance mechanisms and cellular immortalization.

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  1999cited by this paper
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  1998cited by this paper
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  1998cited by this paper
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  1998cited by this paper
• X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

  1998cited by this paper
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  1998cited by this paper
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  1997cited by this paper
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  1997cited by this paper
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  1996cited by this paper
• Dyskeratosis congenita: an inherited bone marrow failure syndrome.

  1996cited by this paper
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  1995cited by this paper
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  1995cited by this paper
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  1995cited by this paper
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  1994cited by this paper
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  1994cited by this paper
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  1993cited by this paper
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  1992cited by this paper
• Dyskeratosis Congenita: Clinical and Genetic Heterogeneity Report of a New Case and Review of the Literature

  1992cited by this paper
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  1977cited by this paper
• Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.

  1975cited by this paper

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