Progressive extreme heterotopic calcification-Reference-Cited by-同舟云学术

Progressive extreme heterotopic calcification

Published:2013-05-17 Issue:7 Volume:161 Page:1706-1713
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Silengo Margherita¹,Defilippi Claudio²,Belligni Elga¹,Biamino Elisa¹,Flex Elisabetta³,Brusco Alfredo⁴,Ferrero Giovanni Battista¹,Tartaglia Marco³,Hennekam Raoul C.⁵

Affiliation:

1. Dipartimento di Scienze della Sanità Pubblica e Pediatriche; Università di Torino; Torino; Italy

2. Dipartimento di Radiologia; AO Città della Salute e della Scienza; Torino; Italy

3. Dipartimento di Ematologia; Oncologia e Medicina Molecolare, Istituto Superiore di Sanità; Roma; Italy

4. Dipartimento di Scienze Mediche; Università di Torino; Torino; Italy

5. Department of Pediatrics and Clinical Genetics; Academic Medical Center, University of Amsterdam; Amsterdam; Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35944/fullpdf

Reference20 articles.

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2. An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia;Benet-Pages;Hum Mol Genet,2005

3. Treatment of heterotopic ossification by extracorporeal shock wave: 26 patients;Brissot;Ann Readapt Med Phys,2005

4. A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis;Ichikawa;J Clin Invest,2007

5. Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1;Kaplan;Hum Mutat,2009

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