MARATTO

article · Gene Reports

First nonsense variant of MED12 gene in a female with complete Maat-Kievit-Brunner phenotype of Ohdo syndrome: A case report

In plain language

No abstract is available for this record, so no summary has been generated.

Research topics

  • Cell Adhesion Molecules Research
  • Cancer-related molecular mechanisms research
  • Signaling Pathways in Disease

Sustainable Development Goals

Read the original research

This page summarises published work. The authoritative version sits with the publisher.

DOI: 10.1016/j.genrep.2024.102005

Is something wrong with this record? Report it or request removal.

Discussion

Discuss this research

Have you built on this work, tried to replicate it, or seen it applied in practice? Share what you know. Verified researchers and MARATTO™ domain experts can open a discussion, and any member can reply. Contributions are reviewed before they appear.

No discussion yet. Open the first thread.