A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
Annals of Dermatology
; : S12-S13, 2019.
Article
in En
| WPRIM
| ID: wpr-762420
Responsible library:
WPRO
ABSTRACT
No abstract available.
Full text:
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Index:
WPRIM
Main subject:
Hyaline Fibromatosis Syndrome
/
Hyalin
Language:
En
Journal:
Annals of Dermatology
Year:
2019
Type:
Article