Brief report: A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features

Hilde Van Esch, Anil K. Agarwal, Philippe Debeer, Jean Pierre Fryns, Abhimanyu Garg

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Fingerprint

Dive into the research topics of 'Brief report: A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features'. Together they form a unique fingerprint.

Medicine & Life Sciences

Chemical Compounds