How to distinguish between autosomal dominant optic atrophy and Leber's hereditary optic neuropathy;Autosomal-Dominant Erbliche Optikusatrophie vs. Lebersche Optikusneuropathie - Wie Kann man sie Unterscheiden?

Ophthalmologe

Volumn 104, Issue 12, 2007, Pages 1060-1065

  Leo Kottler, B ^a,b   Jagle H ^a   Kupker T ^a   Schimpf, S ^a  

^a Universitätsaugenklinik   (Germany)

^b UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

Autosomal dominant optic atrophy; Hereditary optic atrophy; Identification of ADOA and LHON patients; Leber's hereditary optic neuropathy; Molecular genetic analysis

Indexed keywords

EID: 37349036990     PISSN: 0941293X     EISSN: 14330423     Source Type: Journal    
DOI: 10.1007/s00347-007-1577-y     Document Type: Article

References (7)

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3. Internetseite hierzu: www.eOPA1
4. Leo-Kottler B, Christ-Adler M, Reck B et al. (1995) Korrelation klinischer und molekulargenetischer Befunde bei Leberscher Optikusneuropathie. Ophthalmologe 92: 86-92
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6. Pesch UE, Leo-Kottler B, Mayer S et al. (2001) OPA 1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance. Hum Mol Genet 10: 1359-1368
7. Yen MY, Wang AG, Wei YH (2006) Leber's hereditary optic neuropathy: a multifactorial disease. Progress in retinal and eye research 25: 381-396