Systemic Hyalinosis With Heterozygous CMG2 Mutations
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Dermatology,General Medicine,Pathology and Forensic Medicine
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3. Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation;American Journal of Case Reports;2022-05-18
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