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Items: 4

1.
Slowly Progressive Encephalopathy with Hearing Loss Due to a Mutation in the mtDNA tRNALeu(CUN) Gene
Jorida Çoku, Sara Shanske, Mahsa Mehrazin, Kurenai Tanji, Ali Naini, Valentina Emmanuele, Marc Patterson, Michio Hirano, Salvatore DiMauro
J Neurol Sci. Author manuscript; available in PMC 2014 Jan 14.
Published in final edited form as: J Neurol Sci. 2010 Mar 15; 290(0): 166–168. Published online 2009 Dec 22. doi: 10.1016/j.jns.2009.12.001
PMCID:
PMC3891822
ArticlePubReaderPDF–339KCite
2.
Inherited Mitochondrial Diseases of DNA Replication
William C. Copeland
Annu Rev Med. Author manuscript; available in PMC 2008 Mar 21.
Published in final edited form as: Annu Rev Med. 2008; 59: 131–146. doi: 10.1146/annurev.med.59.053006.104646
PMCID:
PMC2271032
ArticlePubReaderPDF–1.2MCite
3.
Clinical and laboratory findings in referrals for mitochondrial DNA analysis
P Lamont, R Surtees, C Woodward, J Leonard, N Wood, A Harding
Arch Dis Child. 1998 Jul; 79(1): 22–27. doi: 10.1136/adc.79.1.22
PMCID:
PMC1717633
SummaryPDF–115KCite
4.
Germ-line deletions of mtDNA in mitochondrial myopathy.
J Poulton, M E Deadman, S Ramacharan, R M Gardiner
Am J Hum Genet. 1991 Apr; 48(4): 649–653.
PMCID:
PMC1682963
SummaryPage BrowsePDF–784KCite

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