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A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia.
J Neurol. 1998 Nov;245(11):755-8. doi: 10.1007/s004150050283.
J Neurol. 1998.
PMID: 9808249
No abstract available.
Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.
Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G.
Comi GP, et al. Among authors: franceschina l.
Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119.
Ann Neurol. 1998.
PMID: 9450776
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Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
Hadjigeorgiou GM, Comi GP, Bordoni A, Shen J, Chen YT, Salani S, Toscano A, Fortunato F, Lucchiari S, Bresolin N, Rodolico C, Piscaglia MG, Franceschina L, Papadimitriou A, Scarlato G.
Hadjigeorgiou GM, et al. Among authors: franceschina l.
J Inherit Metab Dis. 1999 Aug;22(6):762-3. doi: 10.1023/a:1005572906807.
J Inherit Metab Dis. 1999.
PMID: 10472540
No abstract available.
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