Associated Papers
Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review.
Zhu Y et al.
Molecular Genetics & Genomic Medicine, 2022
35726349 (PubMed )
Supplement: MGG3-10-e1993-s001.docx
Protein-losing enteropathy and joint contractures caused by a novel homozygous ANTXR2 mutation.
Schussler E et al.
Advances in Genomics and Genetics, 2018
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