A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects-Reference-Cited by-同舟云学术

A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects

Published:2008-11-05 Issue:5 Volume:17 Page:565-572
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Tuysuz Beyhan,Mosig Rebecca,Altun Gürkan,Sancak Selim,Glucksman Marc J,Martignetti John A

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2008204.pdf

Reference30 articles.

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3. Al Aqeel A, Al Sewairi W, Edress B, Gorlin RJ, Desnick RJ, Martignetti JA : Inherited multicentric osteolysis with arthritis: a variant resembling torg syndrome in a saudi family. Am J Med Genet 2000; 93: 11–18.

4. Al-Mayouf SM, Majeed M, Hugosson C, Bahabri S : New form of idiopathic osteolysis: nodulosis, arthropathy and osteolysis (NAO) syndrome. Am J Med Genet 2000; 93: 5–10.

5. Hall CM : International nosology and classification of constitutional disorders of bone (2001). Am J Med Genet 2002; 113: 65–77.

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