A novel heterozygous missense variant in ribosomal protein L21 associated with familial hypotrichosis simplex
A novel heterozygous missense variant in ribosomal protein L21 associated with familial hypotrichosis simplex
About this course
- Released:
- Expires: June 17, 2028
Target Audience
This activity is intended for practicing dermatologists and other physicians involved in the treatment and management of diseases of the skin.
Learning Objective
To demonstrate up-to-date knowledge of the pathogenesis of hypotrichosis simplex of the scalp
Accreditation and Designation Statement
Once the test is passed, a certificate of completion will be generated. The learning activity can be added to the Royal College of Physicians' CPD diary as a self-certified entry.
Activity Disclosures
No commercial support has been accepted related to the development or publication of this activity.