Associated Papers
Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran.
Goleyjani Moghadam M et al.
Archives of Iranian Medicine, 2023
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment.
Okur V et al.
European Journal of Human Genetics : Ejhg, 2019
A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa.
Sullivan LS et al.
Investigative Ophthalmology & Visual Science, 2014
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