Publications by authors named "Laura Harrold"

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Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation.
Zain Dardas, Laura Harrold, Daniel G Calame, Claire G Salter, Takashi Kikuma

Am J Hum Genet· May 2025

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TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Luis Carlos Tábara, Fatema Al-Salmi, Reza Maroofian, Amna Mohammed Al-Futaisi, Fathiya Al-Murshedi, Laura Harrold

Brain· September 2022

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