Niklas Darín

Researcher Next ID · RN-034653

Researcher · Biochemistry, Genetics and Molecular Biology

Gothenburg, Sweden

Accepting doctoral researchersFunding unknown

Research interests

Biochemistry, Genetics and Molecular Biology

Medicine

Mitochondrial Function and Pathology

Metabolism and Genetic Disorders

Muscle Physiology and Disorders

Neurogenetic and Muscular Disorders Research

Cardiomyopathy and Myosin Studies

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Nature Genetics · 2016 · https://doi.org/10.1038/ng.3740
Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy
New England Journal of Medicine · 2011 · https://doi.org/10.1056/nejmoa1011367
FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study
The Lancet Neurology · 2011 · https://doi.org/10.1016/s1474-4422(11)70155-7
The in-depth evaluation of suspected mitochondrial disease
Molecular Genetics and Metabolism · 2008 · https://doi.org/10.1016/j.ymgme.2007.11.018
Mitochondrial Disease: A Practical Approach for Primary Care Physicians
PEDIATRICS · 2007 · https://doi.org/10.1542/peds.2007-0391
The incidence of mitochondrial encephalomyopathies in childhood: Clinical features and morphological, biochemical, and DNA abnormalities
Annals of Neurology · 2001 · https://doi.org/10.1002/ana.75
Cortisol secretion in relation to body fat distribution in obese premenopausal women
Metabolism · 1992 · https://doi.org/10.1016/0026-0495(92)90171-6

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