Hutchinson?Gilford progeria syndrome with severe skin calcinosis
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2007.02432.x/fullpdf
Reference10 articles.
1. A Case of Hutchinson-Gilford Progeria Syndrome Mimicking Scleredema in Early Infancy
2. Progeria Infantum (Hutchinson–Gilford Syndrome) Associated with Scleroderma‐Like Lesions and Acro‐Osteolysis: A Case Report and Brief Review of the Literature
3. Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
4. A progeroid syndrome in mice is caused by defects in A-type lamins
5. Lamin A Truncation in Hutchinson-Gilford Progeria
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1. Diseases of Collagen and Elastic Tissue;Pediatric Dermatopathology;2017
2. Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome;Brain and Development;2013-08
3. Errors in Metabolism;Andrews' Diseases of the Skin;2011
4. 11 Disorders of collagen;Weedon's Skin Pathology;2010
5. Disorders of collagen;Weedon's Skin Pathology;2010
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