Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy-Reference-Cited by-同舟云学术

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Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy

Published:1991-10 Issue:6 Volume:87 Page:725-727
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Carducci Carla,Leuzzi Vincenzo,Scuderi Massimo,De Negri Anna Maria,Gabrieli Corrado Balacco,Antonozzi Italo,Pontecorvi Alfredo

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00201733.pdf

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. LHON mutations in Italian patients affected by multiple sclerosis;Acta Neurologica Scandinavica;2009-01-29

2. Childhood leber’s hereditary optic neuropathy (ND1/3460) with visual recovery;Pediatric Neurology;1998-10

3. Screening of mtDNA mutations in Italian LHON pedigrees;Journal of Inherited Metabolic Disease;1996-03

4. Leber′s Hereditary Optic Neuropathy (LHON)-Related Mitochondrial DNA Sequence Changes in Italian Patients Presenting with Sporadic Bilateral Optic Neuritis;Biochemical and Molecular Medicine;1995-10

5. Heteroplasmy in Leber's Hereditary Optic Neuropathy;Archives of Ophthalmology;1993-11-01

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