MARATTO

erratum · Journal of Pediatric Genetics

Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1

In plain language

The abstract on record is too brief for a reliable plain-language summary, so none has been generated.

Abstract

[This corrects the article DOI: 10.1055/s-0041-1732474.].

Research topics

  • Bone health and treatments

Read the original research

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

DOI: 10.1055/s-0044-1788343

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.