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Camurati Engelmann disease, type 2
Known as:
CAEND2
, CAMURATI-ENGELMANN DISEASE, TYPE 2
, Progressive diaphyseal dysplasia with striations of the bones
National Institutes of Health
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Related topics
Related topics
3 relations
Autosomal dominant inheritance
Porokeratosis, Disseminated Superficial Actinic
Broader (1)
Camurati-Engelmann Syndrome
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2002
2002
Domain-specific mutations of a transforming growth factor(TGF)-β1 latency-associated peptide cause Camurati-Engelmann disease because of the formation of a constitutively active form of TGF-β1
齊藤 貴志
2002
Corpus ID: 87000391
Highly Cited
2001
Highly Cited
2001
Domain-specific Mutations of a Transforming Growth Factor (TGF)-β1 Latency-associated Peptide Cause Camurati-Engelmann Disease Because of the Formation of a Constitutively Active Form of TGF-β1*
T. Saito
,
A. Kinoshita
,
+5 authors
N. Taniguchi
Journal of Biological Chemistry
2001
Corpus ID: 28803006
Transforming growth factor (TGF)-β1 is secreted as a latent form, which consists of its mature form and a latency-associated…
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