Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A-Reference-Cited by-同舟云学术

Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A

Published:2011-11-07 Issue:12 Volume:155 Page:3002-3006
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hisama Fuki M.,Lessel Davor,Leistritz Dru,Friedrich Katrin,McBride Kim L.,Pastore Matthew T.,Gottesman Gary S.,Saha Bidisha,Martin George M.,Kubisch Christian,Oshima Junko

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. LMNA mutations in atypical Werner's syndrome;Chen;Lancet,2003

2. Lamin a truncation in Hutchinson-Gilford progeria;De Sandre-Giovannoli;Science,2003

3. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome;Eriksson;Nature,2003

4. WRN mutations in Werner syndrome patients: Genomic rearrangements, unusual intronic mutations and ethnic-specific alterations;Friedrich;Hum Genet,2010

5. LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome;Fukuchi;J Med Genet,2004

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