Atlas Trials

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

Clinical trial NCT02509650 · UNKNOWN

Trial details

NCT number
NCT02509650
Sponsor
University Hospital, Strasbourg, France
Status
UNKNOWN
Study type
OBSERVATIONAL
Familial LipomatosisVery Rare Dermatologic Diseases
Start date
2015-09-01
Primary completion
2018-02-01
Enrollment
25

View on ClinicalTrials.gov

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