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- NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_assertion type Assertion NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_head.
- NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_assertion wasGeneratedBy ECO_0000203 NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_provenance.
- NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_assertion wasDerivedFrom befree-20140225 NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_provenance.
- NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_assertion SIO_000772 16278265 NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_provenance.
- NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_assertion evidence source_evidence_literature NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_provenance.
- NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_assertion description "[The S573L homozygous LMNA mutation is associated with a novel phenotype of arthropathy, tendinous calcifications, and progeroid features distinct from the acroosteolysis previously reported in patients with mandibuloacral dysplasia caused by LMNA or ZMPSTE24 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569291.RA8Jm66S6Dj6ZzfsDZ2CYJhICpEEj6XlXgNBqeqH9guLs130_provenance.