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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and RRM2B[original query]
Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia.
Brain : a journal of neurology 2014 Dec 137 (Pt 12): 3200-12.
Horga Alejandro, Pitceathly Robert D S, Blake Julian C, Woodward Catherine E, Zapater Pedro, Fratter Carl, Mudanohwo Ese E, Plant Gordon T, Houlden Henry, Sweeney Mary G, Hanna Michael G, Reilly Mary
Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.
Mitochondrion 2015 Dec 26 81-85.
Paramasivam Arumugam, Meena Angamuthu Kannan, Pedaparthi Lalitha, Jyothi Vuskamalla, Uppin Megha S, Jabeen Shaikh Afshan, Sundaram Challa, Thangaraj Kumarasa
Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study.
Neurology. Clinical practice 2021 4 11 (2): 97-104.
Braz Luis P, Ng Yi Shiau, Gorman Gráinne S, Schaefer Andrew M, McFarland Robert, Taylor Robert W, Turnbull Doug M, Whittaker Roger
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