Associated Papers
Human missense variants in F3 impair the initiation of blood coagulation.
Ansari SA et al.
Blood, 2025
Tissue-specific mitochondrial DNA, MT-TF, pathogenic variants in mitochondrial myopathies.
Rose S et al.
Molecular Genetics and Metabolism Reports, 2025
New-Onset Refractory Status Epilepticus Due to a Novel MT-TF Variant: Time for Acute Genetic Testing Before Treatment?
Indelicato E et al.
Neurology. Genetics, 2023
Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF.
Finsterer J
Molecular Genetics and Metabolism Reports, 2019
Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF.
Barcia G et al.
Molecular Genetics and Metabolism Reports, 2019
Mitochondrial disease--an important cause of end-stage renal failure.
Rahman S et al.
Pediatric Nephrology (berlin, Germany), 2013
A naturally occurring polymorphism at Drosophila melanogaster Lim3 Locus, a homolog of human LHX3/4, affects Lim3 transcription and fly lifespan.
Rybina OY et al.
Plos One, 2010
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