Mild Myopathy Is Associated with COMP but Not MATN3 Mutations in Mouse Models of Genetic Skeletal Diseases
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference65 articles.
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1. Structure, evolution and expression of zebrafish cartilage oligomeric matrix protein (COMP, TSP5). CRISPR-Cas mutants show a dominant phenotype in myosepta;Frontiers in Endocrinology;2022-11-14
2. Loss of Smad4 in the scleraxis cell lineage results in postnatal joint contracture;Developmental Biology;2021-02
3. Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia;The Journal of Gene Medicine;2019-07-11
4. Cartilage oligomeric matrix protein: COMPopathies and beyond;Matrix Biology;2018-10
5. Skeletal Dysplasias;Genetics of Bone Biology and Skeletal Disease;2018
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