Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucomaTIN AUNG; OCAKA, Louise; EBENEZER, Neil D et al.Human genetics. 2002, Vol 110, Num 5, pp 513-514, issn 0340-6717Article

Mutation spectrum and splicing variants in the OPA1 geneDELETTRE, Cécile; GRIFFOIN, Jean-Michel; KAPLAN, Josseline et al.Human genetics. 2001, Vol 109, Num 6, pp 584-591, issn 0340-6717Article

OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritancePESCH, Ulrike E. A; LEO-KOTTLER, Beate; MAYER, Simone et al.Human molecular genetics (Print). 2001, Vol 10, Num 13, pp 1359-1368, issn 0964-6906Article

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28ALEXANDER, Christiane; VOTRUBA, Marcela; BHATTACHARYA, Shomi S et al.Nature genetics. 2000, Vol 26, Num 2, pp 211-215, issn 1061-4036Article

A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophyTHISELTON, Dawn L; ALEXANDER, Christiane; BHATTACHARYA, Shomi S et al.Investigative ophthalmology & visual science. 2002, Vol 43, Num 6, pp 1715-1724, issn 0146-0404Article

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I: Linkage analysisEIBERG, H; KJER, B; KJER, P et al.Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 977-980, issn 0964-6906Article

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyTOOMES, Carmel; MARCHBANK, Nicola J; TEIMORY, Masoud et al.Human molecular genetics (Print). 2001, Vol 10, Num 13, pp 1369-1378, issn 0964-6906Article

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyDELETTRE, Cécile; LENAERS, Guy; ASTARIE-DEQUEKER, Catherine et al.Nature genetics. 2000, Vol 26, Num 2, pp 207-210, issn 1061-4036Article