A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome-Reference-Cited by-同舟云学术

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A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome

Published:2024-09 Issue: Volume:22 Page:101789
ISSN:2352-1872
Container-title:Bone Reports
language:en
Short-container-title:Bone Reports

Author:

Ahmad Safeer,Muurinen Mari,Loid Petra,Ali Muhammad Zeeshan,Muzammal Muhammad,Fatima Sana,Khan Jabbar,Khan Muzammil Ahmad,Mäkitie Outi

Publisher

Elsevier BV

Reference45 articles.

1. Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family;Al Aqeel;Am. J. Med. Genet.,2000

2. Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy;Azzollini;J. Hum. Genet.,2014

3. Mutation in MMP2 gene may result in scleroderma-like skin thickening;Bader-Meunier;Ann. Rheum. Dis.,2016

4. Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy;Bhavani;Am. J. Med. Genet. A,2016

5. Multicentric Osteolysis Nodulosis and Arthropathy;Bhavani,2021

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