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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

Related topics

Related topics

3 relations
Autosomal dominant inheritancePorokeratosis, Disseminated Superficial Actinic

Broader (1)

Camurati-Engelmann Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
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
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