Morten Duno

10PUBLICATIONS
39CO-AUTHORS
Molecular imaging (incl. electron microscopy and neutron diffraction)Metabolic medicineGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesPolymerisation mechanisms
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Journal

Publications (10)

|Nov 04, 2026
Two Additional Variants Expand the Genotypic Spectrum of Dominant Calpain-3 Deficiencies.

|Mar 19, 2026
m.10010T>C Mitochondrial Disease: A Case Report With Hypoparathyroidism and Review of the Literature.

Jacob Mohr, Anja Lisbeth Frederiksen, Morten Duno

|Jan 22, 2026
Genetic diagnosis of CYP21A2-related CAH: adaptive sampling long-read sequencing is an accurate and scalable solution.

Dorte Launholt Lildballe, Morten Reiffenstein Huno, Lukas Ochsner Reynaud Ridder

|Dec 24, 2025
Systematic Review on Genetic Variants in Children With Cerebral Palsy.

Signe V Pedersen, Jesper K Sørensen, Rebecca Fabricius

|Aug 04, 2025
Clinical and Genetic Reassessment in Patients With Clinically Diagnosed Hereditary Polyneuropathy.

Louise Sloth Kodal, Morten Duno, Tina Dysgaard

|Apr 14, 2025
Variants in CAPN3 Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy Combined With Calpain-3 Deficiency.

Thomas Krag, Emily Nasho, Lauren Brady

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Frequent Collaborators

2 joint publications

John Vissing

2 joint publications

Thomas Krag

2 joint publications

Claus Højbjerg Gravholt

1 joint publications

Nanna Witting