Gonda 8-104/Joseph 1-242
Muscle
Stefan Nicolau, M.D., M.Ch.
"Phenotypic Variability in Inherited Myopathies: Still Searching for Answers"
Learning objectives:
- Identify genetic and epigenetic sources of phenotypic variability in common inherited myopathies
- Describe recent advances in understanding the mechanisms of congenital myotonic dystrophy and FSHD
- Assess the impact of phenotypic variability on clinical trial development
The presenter (nor spouse/partner) does not have a relevant financial relationship to disclose and does not intend to discuss an off-label/investigative use of a commercial product/device.
For disclosure information regarding Mayo Clinic School of Continuous Professional Development accreditation review committee member(s), please go here.
ATTENDANCE/CREDIT
Text the session code (provided only at the session) to 507-200-3010 within 48 hours of the live presentation to record attendance. All learners are encouraged to text attendance regardless of credit needs. This number is only used for receiving text messages related to tracking attendance. Additional tasks to obtain credit may be required based on the specific activity requirements and will be announced accordingly. Swiping your badge will not provide credit; that process is only applicable to meet GME requirements for Residents & Fellows.
TRANSCRIPT
Any credit or attendance awarded from this series will appear on your Transcript.

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