Aberrant Signal Peptide Cleavage of Collagen X in Schmid Metaphyseal Chondrodysplasia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference25 articles.
1. Type X Collagen Multimer Assembly in Vitro Is Prevented by a Gly618 to Val Mutation in the α1(X) NC1 Domain Resulting in Schmid Metaphyseal Chondrodysplasia
2. The human collagen X gene. Complete primary translated sequence and chromosomal localization
3. Phenotypic and biochemical consequences of collagen X mutations in mice and humans
4. The fibrillar collagens, collagen VIII, collagen X and the C1q complement proteins share a similar domain in their C‐terminal non‐collagenous regions
5. A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
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