Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription.

No abstract is available for this paper.

• Publication year

  2003

• Venue

  Experimental Cell Research

• Publication date

  2003-11-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/S0014-4827(03)00395-1PMID 14597414
• 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.

• LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)

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  1999cited by this paper
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