Franclo Henning

10PUBLICATIONS
93CO-AUTHORS
Neurology and neuromuscular diseasesOptical technologyGene expression (incl. microarray and other genome-wide approaches)Metabolic medicineMajor global burdens of disease
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Publications (10)

|Jan 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.

Lydia Sagath, Kirsi Kiiski, Kireshnee Naidu

|Aug 02, 2024
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G Variant.

Franclo Henning, Kireshnee Naidu, Christopher J Record

|Apr 29, 2024
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones

|Jan 14, 2024
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study.

Michelle Bisschoff, Izelle Smuts, Marli Dercksen

|Jul 30, 2023
Neuromuscular disease genetics in under-represented populations: increasing data diversity.

Lindsay A Wilson, William L Macken, Luke D Perry

|Dec 14, 2022
Preservation of shortening velocity and power output in single muscle fibres from patients with idiopathic inflammatory myopathies.

Franclo Henning, Tertius Abraham Kohn

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