Infantile systemic hyalinosis: a case report and mutation analysis in a Chinese infant
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2006.07701.x/fullpdf
Reference5 articles.
1. Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
2. Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
3. Infantile Systemic Hyalinosis: Report of Four Cases of a Disease, Fatal in Infancy, Apparently Different from Juvenile Systemic Hyalinosis
4. Two Siblings with Juvenile Hyaline Fibromatosis: Case Reports and Review of the Literature
5. Differential gene expression during capillary morphogenesis in 3D collagen matrices
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