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Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation.
10.1002/mgg3.1203
000520746400001
32196989
Härter
B.
author
Benedicenti
F.
author
Karall
D.
author
Lausch
E.
author
Schweigmann
G.
author
Stanzial
F.
author
Superti-Furga
A.
author
Scholl-Bürgi
S.
author
article
casereport
2020-06
Molecular genetics & genomic medicine
2324-9269
2324-9269
journal
8
6
e1203
ANTXR2
CMG2
Hyaline Fibromatosis Syndrome
infantile systemic hyalinosis
juvenile hyaline fibromatosis
ANTXR2
CMG2
eng
60_published
true
peer-reviewed
Publication types: Journal Article
Publication Status: ppublish
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