Two novel compound heterozygous anthrax toxin receptor 2 mutations in a Chinese patient with hyaline fibromatosis syndrome
Author:
Affiliation:
1. Department of Dermatology and Venereology First Affiliated HospitalGuangxi Medical University Nanning China
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.15353
Reference5 articles.
1. Infantile Systemic Hyalinosis: A Case Report of Compromised Cellular and Humoral Branches of the Immune System Leading to Infections
2. Juvenile hyaline fibromatosis: impaired collagen metabolism in human skin fibroblasts
3. Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system
4. Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations
5. Infantile systemic hyalinosis in identical twins
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