Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
- 1 October 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 73 (4) , 791-800
- https://doi.org/10.1086/378418
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21American Journal of Human Genetics, 2002
- Identification of the cellular receptor for anthrax toxinNature, 2001
- Hyaline FibromatosisAdvances in Anatomic Pathology, 2001
- Genes Expressed in Human Tumor EndotheliumScience, 2000
- Two Siblings with Juvenile Hyaline Fibromatosis: Case Reports and Review of the LiteratureClinical Rheumatology, 1999
- Skin collagen defects in a patient with juvenile hyaline fibromatosis.Archives of Disease in Childhood, 1995
- Clinical, Histologic, and Ultrastructural Findings in Two Cases of Infantile Systemic HyalinosisPediatric Dermatology, 1992
- Infantile Systemic Hyalinosis: Report of Four Cases of a Disease, Fatal in Infancy, Apparently Different from Juvenile Systemic HyalinosisPediatric Pathology, 1986
- Systemic hyalinosis or juvenile hyaline fibromatosisArchives of Dermatological Research, 1980
- Systemic hyalinosis (juvenile hyaline fibromatosis)Archives of Dermatological Research, 1979