Clinical Trial Update: Identification of Mutations Responsible for Rare Familial Skin Diseases by Next Generation Sequencing

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Summary

A clinical trial update from University Hospital Strasbourg describes efforts to identify mutations responsible for rare familial skin diseases using next-gener…

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Diseases / indications

• Familial Lipomatosis

Snippet

Sponsor: University Hospital, Strasbourg, France | Conditions: Familial Lipomatosis, Very Rare Dermatologic Diseases | Status: UNKNOWN