Publications by authors named "Annika Neethling"

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A South African family with myoclonus-dystonia syndrome with a novel mutation in the SGCE gene responding to deep brain stimulation.
Riaan van Coller, Soraya Bardien, Annika Neethling, Jonathan Carr, Clara Schutte

Parkinsonism Relat Disord· November 2019

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Wild-type and mutant (G2019S) leucine-rich repeat kinase 2 (LRRK2) associate with subunits of the translocase of outer mitochondrial membrane (TOM) complex.
Annika Neethling, Lize Engelbrecht, Ben Loos, Craig Kinnear, Rensu Theart

Exp Cell Res· February 2019

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Underappreciated Roles of the Translocase of the Outer and Inner Mitochondrial Membrane Protein Complexes in Human Disease.
Thea Heinemeyer, Monique Stemmet, Soraya Bardien, Annika Neethling

DNA Cell Biol· January 2019

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Exome sequencing identifies a novel TTC37 mutation in the first reported case of Trichohepatoenteric syndrome (THE-S) in South Africa.
Craig Kinnear, Brigitte Glanzmann, Eric Banda, Nikola Schlechter, Glenda Durrheim, Annika Neethling

BMC Med Genet· March 2017

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Filamin C: a novel component of the KCNE2 interactome during hypoxia.
Annika Neethling, Jomien Mouton, Ben Loos, Valerie Corfield, Carin de Villiers

Cardiovasc J Afr· December 2016

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