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Clinical trial

Identification of Mutations Responsible for Rare Familial Skin Diseases by Next Generation Sequencing

NCT02509650 is registered in ClinicalTrials.gov with University Hospital, Strasbourg, France as lead sponsor.

NCT NCT02509650
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Registry record

As filed in ClinicalTrials.gov.

Title
Identification of Mutations Responsible for Rare Familial Skin Diseases by Next Generation Sequencing
Lead sponsor
University Hospital, Strasbourg, France
Phase
Observational
Overall status
Unknown status
Start date
September 30, 2015
Completion date
February 28, 2018
Enrollment
25 (estimated)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.

familial lipomatosis, very rare dermatologic diseases