Screening of mtDNA mutations in Italian LHON pedigrees
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF01799410
Reference6 articles.
1. Brown MD, Wallace DC (1994) Molecular basis of mitochondrial DNA disease.J Bioenerg Biomembr 26: 273–289.
2. Carducci C, Leuzzi V, Scuderi M, et al (1991) Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.Hum Genet 87: 725–728.
3. Gerbitz KD, Paprotta A, Obermaier-Kusser B, et al (1992) No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA mutations associated with LHON.FEBS 3: 251–255.
4. Mackey D, Nasioulas S, Forrest S (1993) Finger prick blood testing in Leber hereditary optic neuropathy.Br J Ophthalmol 77: 311–312.
5. Newman N, Torroni A, Brown MD, et al (1994) Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients.Am J Ophthalmol 118: 158–168.
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