Amica Corda Müller-Nedebock

3PUBLICATIONS
4CO-AUTHORS
CrystallographyNeurology and neuromuscular diseasesPharmacogenomics
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Publications (3)

|Jul 29, 2025
Uniparental disomy leads to a novel cause of MC2R-related familial glucocorticoid deficiency type 1.

Amica Corda Müller-Nedebock, Eric Wenzel, Roland Pfäffle

|Jul 06, 2021
Copy Number Variation in Parkinson's Disease: An Update from Sub-Saharan Africa.

Amica C Müller-Nedebock, Morenikeji A Komolafe, Michael B Fawale

|Jan 29, 2021
Nuclear Genes Associated with Mitochondrial DNA Processes as Contributors to Parkinson's Disease Risk.

Amica C Müller-Nedebock, Francois H van der Westhuizen, Sulev Kõks

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