The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene

Author: Amati-Bonneau P.   Odent S.   Derrien C.   Pasquier L.   Malthiery Y.   Reynier P.   Bonneau D.  

Publisher: Elsevier

ISSN: 0002-9394

Source: American Journal of Ophthalmology, Vol.136, Iss.6, 2003-12, pp. : 1170-1171

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